(352 days)
No
The summary describes a standard immunoassay with no mention of AI or ML terms, image processing, or training/test data sets typically associated with AI/ML models.
No
The device is an in vitro diagnostic (IVD) test intended for the semi-quantitative measurement of antibodies as an aid in diagnosis, not for treatment or prevention of disease.
Yes
The "Intended Use / Indications for Use" states that the device is intended "as an aid in the diagnosis of systemic lupus erythematosus (SLE)".
No
The device description explicitly states it is a "semi-quantitative solid-phase fluoroimmunoassay" and includes "assay-specific reagents, EliA method-specific reagents, and general reagents," indicating it is a hardware-based in vitro diagnostic device that utilizes chemical reactions and fluorescence detection, not a software-only device.
Yes, this device is an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The "Intended Use / Indications for Use" section explicitly states that the device is "intended for the in vitro semi-quantitative measurement of IgG antibodies directed to Sm in human serum and EDTA-plasma". The term "in vitro" is a key indicator of an IVD, meaning it's used to test samples outside of the living body.
- Device Description: The description mentions it's a "solid-phase fluoroimmunoassay, for the determination of autoantibodies against Sm". Immunoassays are a common type of test used in IVDs to detect specific substances in biological samples.
- Sample Type: The intended use specifies the use of "human serum and EDTA-plasma", which are biological samples commonly tested in IVD procedures.
- Aid in Diagnosis: The intended use states it's "as an aid in the diagnosis of systemic lupus erythematosus (SLE)". IVDs are used to provide information that assists in the diagnosis of diseases.
All of these points align with the definition and characteristics of an In Vitro Diagnostic device.
N/A
Intended Use / Indications for Use
EliA SmDP-S is intended for the in vitro semi-quantitative measurement of IgG antibodies directed to Sm in human serum and EDTA-plasma as an aid in the diagnosis of systemic lupus erythematosus (SLE) in conjunction with other laboratory and clinical findings. EliA SmDP-S uses the EliA IgG method.
Product codes (comma separated list FDA assigned to the subject device)
LKP
Device Description
The EliA SmD -S is a semi-quantitative solid-phase fluoroimmunoassay, for the determination of autoantibodies against Sm. The EliA SmDP-S test System is fully integrated and automated system which comprises of assay-specific reagents, EliA method-specific reagents, and general reagents.
Assav-Specific Reagents include:
- EliA SmD -S Wells: coated with a synthetic SmD3 peptide 4 carriers (16 wells . each), ready to use;
- . EliA ANA Positive Controls: Human blood preparation containing IgG antibodies to dsDNA, RNP, Sm, Ro, La, Scl-70, CENP and Jo-1 in PBS containing BSA, detergent and 0.095% sodium azide - 6 single use vials, 0.3 mL each, ready to use:
- . EliA IgG/IgM/IgA Neqative Control 250 or 2500/5000: Human blood preparation from healthy donors in PBS containing BSA, detergent and 0.095% sodium azide - 6 single-use vials, 0.3 mL each, ready to use;
EliA Method-Specific Reagents include:
- . EliA Sample Diluent: PBS containing BSA, detergent and 0.095% sodium azide -6 bottles, 48 mL each, ready to use; or 6 bottles, 400 mL each, ready to use;
- . EliA IgG Conjugate 50 or 200: ß-Galactosidase labeled anti-IgG (mouse monoclonal antibodies) in PBS containing BSA and 0.06% sodium azide - 6
- wedge shaped bottles. 5 mL each. ready to use: or 6 wedge shaped bottles. 19 mL each. ready to use:
- . EliA IgG Calibrator Strips: Human IgG (0, 4, 10, 20, 100, 600 µg/L) in PBS containing BSA, detergent and 0.095% sodium azide - 5 strips, 6 single-use vials per strip, 0.3 mL each, ready to use;
- . EliA IgG Curve Control Strips: Human IgG (20 ug/L) in PBS containing BSA, detergent and 0.095% sodium azide - 5 strips, 6 single-use vials per strip, 0.3 mL each, ready to use:
- . EliA IgG Calibrator Well: coated with mouse monoclonal antibodies – 4 carriers (16 wells each), ready to use;
General Reagents include:
- Development Solution: 0.01% 4-Methylumbellifervl-B-D-qalactoside. 110, 6x >170, or 6x >1165 determinations;
- Stop Solution: 4% Sodium Carbonate 6 bottles (65 mL, 119 mL, or 2800 mL . each), sufficient for 6x >292, 6x >560, or 6x >13100 determinations;
- Washing Solution Additive: detergent, preservative 10 EliA U/mL (Positive).
2. Comparison Studies:
- a) Method Comparison with Predicate Device:
- Sample size: 628 patient samples, 460 values within measuring range used for analysis.
- Test: EliA SmDP-S compared to EliA SmDP. Single determination.
- Key results:
- EliA SmDP-S: equivocal results considered negative: Positive Percent Agreement 91.8% (95% CI: 86.9 – 95.4), Negative Percent Agreement 96.7% (95% CI: 93.9 – 98.5), Total Agreement 94.8% (95% CI: 92.3 – 96.6).
- EliA SmDP-S: equivocal results considered positive: Positive Percent Agreement 92.6% (95% CI: 88.3 – 95.7), Negative Percent Agreement 97.1% (95% CI: 94.2 – 98.8), Total Agreement 95.0% (95% CI: 94.2 – 98.8).
- Matrix Comparison:
- Sample size: 93 patients (Serum, Li-heparin plasma, EDTA-plasma). 25 positive samples spiked.
- Test: Serum vs. Li-heparin plasma, and Serum vs. EDTA plasma. Single determination. Passing-Bablok regression.
- Key results:
- Serum vs. Li-heparin plasma: Slope 0.88 (95% CI: 0.84 to 0.92), Intercept -0.31 (95% CI: -0.53 to -0.15), R2 1.00.
- Serum vs. EDTA plasma: Slope 0.99 (95% CI: 0.96 – 1.02), Intercept 0.13 (95% CI: -0.12 to 0.38), R2 1.00.
- Conclusion: Only serum and EDTA plasma are appropriate sample matrices. Heparin can suppress SmD antibody reaction.
- b) Instrument Comparison:
- Sample size: 105 positive, 15 equivocal and 14 negative samples.
- Test: EliA SmDP-S evaluated on Phadia 250 and Phadia 2500E. Single determination. Regression analysis.
- Key results: Intercept -0.73 (95% CI: -1.20 – -0.36), Slope 1.01 (95% CI: 0.98 - 1.03).
3. Clinical Studies:
- a) Clinical Sensitivity and Specificity:
- Sample size: 328 clinically defined samples (Systemic lupus erythematosus (n = 104), mixed connective tissue disease (n = 22), Sjögren's syndrome (n = 28), scleroderma (n = 32), polymyositis/dermatomyositis (n=10), rheumatoid arthritis (n = 52), Graves' disease (n = 10), Hashimoto's disease (n = 10), bacterial infections (n = 30), and viral infections (n=30)).
- Key results:
- EliA SmDP-S - equivocal results evaluated as positive: Sensitivity (95% CI): 18.3% (11.4% - 27.1%), Specificity (95% CI): 98.7% (96.1% - 99.7%).
- EliA SmDP-S - equivocal results evaluated as negative: Sensitivity (95% CI): 18.3% (11.4% - 27.1%), Specificity (95% CI): 99.6% (97.5% - 100%).
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Method Comparison with Predicate Device (EliA SmDP-S: equivocal results considered negative):
- Positive Percent Agreement: 91.8% (95% CI: 86.9 – 95.4)
- Negative Percent Agreement: 96.7% (95% CI: 93.9 – 98.5)
- Total Agreement: 94.8% (95% CI: 92.3 – 96.6)
Method Comparison with Predicate Device (EliA SmDP-S: equivocal results considered positive): - Positive Percent Agreement: 92.6% (95% CI: 88.3 – 95.7)
- Negative Percent Agreement: 97.1% (95% CI: 94.2 – 98.8)
- Total Agreement: 95.0% (95% CI: 94.2 – 98.8)
Clinical Sensitivity and Specificity (equivocal results evaluated as positive): - Sensitivity: 18.3% (95% CI: 11.4% - 27.1%)
- Specificity: 98.7% (95% CI: 96.1% - 99.7%)
Clinical Sensitivity and Specificity (equivocal results evaluated as negative): - Sensitivity: 18.3% (95% CI: 11.4% - 27.1%)
- Specificity: 99.6% (95% CI: 97.5% - 100%)
Predicate Device(s): If the device was cleared using the 510(k) pathway, identify the Predicate Device(s) K/DEN number used to claim substantial equivalence and list them here in a comma separated list exactly as they appear in the text. List the primary predicate first in the list.
Reference Device(s): Identify the Reference Device(s) K/DEN number and list them here in a comma separated list exactly as they appear in the text.
Predetermined Change Control Plan (PCCP) - All Relevant Information for the subject device only (e.g. presence / absence, what scope was granted / cleared under the PCCP, any restrictions, etc).
Not Found
§ 866.5100 Antinuclear antibody immunological test system.
(a)
Identification. An antinuclear antibody immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the autoimmune antibodies in serum, other body fluids, and tissues that react with cellular nuclear constituents (molecules present in the nucleus of a cell, such as ribonucleic acid, deoxyribonucleic acid, or nuclear proteins). The measurements aid in the diagnosis of systemic lupus erythematosus (a multisystem autoimmune disease in which antibodies attack the victim's own tissues), hepatitis (a liver disease), rheumatoid arthritis, Sjögren's syndrome (arthritis with inflammation of the eye, eyelid, and salivary glands), and systemic sclerosis (chronic hardening and shrinking of many body tissues).(b)
Classification. Class II (performance standards).
0
Image /page/0/Picture/0 description: The image shows the logo of the U.S. Food and Drug Administration (FDA). On the left is the Department of Health & Human Services logo. To the right of that is the FDA logo, with the letters "FDA" in a blue square. To the right of the blue square is the text "U.S. FOOD & DRUG ADMINISTRATION" in blue.
July 14, 2021
Phadia AB % Sheryl Skinner Associate Director RA/QA Phadia US Inc. 4169 Commercial Avenue Portage, Michigan 49002
Re: K202067
Trade/Device Name: EliA SmDf-S Regulation Number: 21 CFR 866.5100 Regulation Name: Antinuclear antibody immunological test system Regulatory Class: Class II Product Code: LKP Dated: November 30, 2020 Received: December 1, 2020
Dear Sheryl Skinner:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database located at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal
1
statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801 and Part 809); medical device reporting of medical device-related adverse events) (21 CFR 803) for devices or postmarketing safety reporting (21 CFR 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reportingcombination-products); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems.
For comprehensive regulatory information about medical devices and radiation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medicaldevices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-device-advice-comprehensive-regulatoryassistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100).
Sincerely,
Ying (Katelin) Mao, Ph.D. Chief Division of Immunology and Hematology Devices OHT7: Office of In Vitro Diagnostics and Radiological Health Office of Product Evaluation and Ouality Center for Devices and Radiological Health
Enclosure
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Indications for Use
510(k) Number (if known) K202067
Device Name EliA SmDP-S
Indications for Use (Describe)
EliA SmDP-S is intended for the in vitro semi-quantitative measurement of IgG antibodies directed to Sm in human serum and EDTA-plasma as an aid in the diagnosis of systemic lupus erythematosus (SLE) in conjunction with other laboratory and clinical findings. EliA SmDP-S uses the EliA IgG method.
| Type of Use (Select one or both, as applicable) | |
|---|---|
| X Prescription Use (Part 21 CFR 801 Subpart D) | Over-The-Counter Use (21 CFR 801 Subpart C) |
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510(k) Decision Summary
This 510(k) Summary is prepared in accordance with the requirements of 21 CFR Part 807.92.
Premarket Notification 510(k) No: K202067
| Date of Summary Preparation: | July 14, 2021 |
|---|---|
| Manufacturer: | Phadia AB |
| Rapsgatan 7P | |
| P.O. Box 6460 | |
| 751 37 Uppsala, Sweden | |
| Distributor: | Phadia US Inc. |
| 4169 Commercial Avenue | |
| Portage, MI 49002 | |
| Company Contact Person: | Sheryl Skinner |
| Associate Director Quality and Regulatory | |
| Phadia US Inc. | |
| 4169 Commercial Avenue | |
| (269) 568-3603 | |
| sheryl.skinner@thermofisher.com |
Proprietary and Established Device Name:
EliA SmD²-S
Regulatory Information:
| Product Code: | LKP |
|---|---|
| Classification: | Class II |
| Regulation: | 21 CFR 866.5100 – Antinuclear Antibody Immunological |
| Test System | |
| Panel: | Immunology |
Purpose of Submission:
New Device
Measurand:
IgG autoantibodies specific to Sm protein (Sm) D component
4
Type of Test:
Automated semi-quantitative solid phase fluoroimmunoassay
Intended Use:
EliA SmD -S is intended for the in vitro semi-quantitative measurement of IgG antibodies directed to Sm in human serum and EDTA-plasma as an aid in the diagnosis of systemic lupus erythematosus (SLE) in conjunction with other laboratory and clinical findings. EliASmD -S uses the EliA IgG method.
Indication(s) for Use:
Same as intended use
Special Conditions for Use:
Rx - For Prescription Use Only
Special Instrument Requirements:
For use on the Phadia 250 instrument and the E-module of the Phadia 2500 and Phadia 5000 series of instruments.
Device Description:
The EliA SmD -S is a semi-quantitative solid-phase fluoroimmunoassay, for the determination of autoantibodies against Sm. The EliA SmDP-S test System is fully integrated and automated system which comprises of assay-specific reagents, EliA method-specific reagents, and general reagents.
Assav-Specific Reagents include:
- EliA SmD -S Wells: coated with a synthetic SmD3 peptide 4 carriers (16 wells . each), ready to use;
- . EliA ANA Positive Controls: Human blood preparation containing IgG antibodies to dsDNA, RNP, Sm, Ro, La, Scl-70, CENP and Jo-1 in PBS containing BSA, detergent and 0.095% sodium azide - 6 single use vials, 0.3 mL each, ready to use:
- . EliA IgG/IgM/IgA Neqative Control 250 or 2500/5000: Human blood preparation from healthy donors in PBS containing BSA, detergent and 0.095% sodium azide - 6 single-use vials, 0.3 mL each, ready to use;
EliA Method-Specific Reagents include:
- . EliA Sample Diluent: PBS containing BSA, detergent and 0.095% sodium azide -6 bottles, 48 mL each, ready to use; or 6 bottles, 400 mL each, ready to use;
- . EliA IgG Conjugate 50 or 200: ß-Galactosidase labeled anti-IgG (mouse monoclonal antibodies) in PBS containing BSA and 0.06% sodium azide - 6
5
wedge shaped bottles. 5 mL each. ready to use: or 6 wedge shaped bottles. 19 mL each. ready to use:
- . EliA IgG Calibrator Strips: Human IgG (0, 4, 10, 20, 100, 600 µg/L) in PBS containing BSA, detergent and 0.095% sodium azide - 5 strips, 6 single-use vials per strip, 0.3 mL each, ready to use;
- . EliA IgG Curve Control Strips: Human IgG (20 ug/L) in PBS containing BSA, detergent and 0.095% sodium azide - 5 strips, 6 single-use vials per strip, 0.3 mL each, ready to use:
- . EliA IgG Calibrator Well: coated with mouse monoclonal antibodies – 4 carriers (16 wells each), ready to use;
General Reagents include:
- Development Solution: 0.01% 4-Methylumbellifervl-B-D-qalactoside. 110, 6x >170, or 6x >1165 determinations;
- Stop Solution: 4% Sodium Carbonate 6 bottles (65 mL, 119 mL, or 2800 mL . each), sufficient for 6x >292, 6x >560, or 6x >13100 determinations;
- Washing Solution Additive: detergent, preservative 10 EliA U/mL | Same |
| Differences | | |
| Feature | Proposed Device
EliA SmDP-S | Predicate Device
EliA SmDP |
| Instrument Platforms | Phadia 250, E-module of the Phadia 250 and Phadia 5000 series | Phadia 100, Phadia 250, E-module of the Phadia 250 and Phadia 5000 series |
| Sample type | Serum or EDTA-plasma | Serum, citrate- or EDTA-plasma |
| Sample Dilution | 1:100 | 1:50 |
| Coating Technology | adsorptive coating of a SmD3 peptide-polymer conjugate | affinity-based coating of SmD3 peptide |
Standard/Guidance Document Referenced
- . CLSI EP25-A, Evaluation of Stability of In Vitro Diagnostic Reagents, September 2009
- CLSI EP05-A3, Evaluation of Precision of Quantitative Measurement Procedures, . September 2014
- . CLSI EP6-A, Evaluation of the Linearity of Quantitative Measurement Procedures: A Statistical Approach, April 2003
- CLSI EP07-ED3, Interference Testing in Clinical Chemistry, September 2018
- I CLSI EP37-ED1. Supplemental Tables for Interference Testing, September 2018
- CLSI EP09c-ED3, Measurement Procedure Comparison and Bias Estimation ■ Using Patient Samples, June 2018
- . CLSI EP17-A2, Evaluation of Detection Capability for Clinical Laboratory Measurement Procedures, June 2012
- . CLSI EP28-A3c, Defining, Establishing, and Verifying Reference Intervals in the Clinical Laboratory, October 2010
Test Principle
The EliA tests are fluorescence immunoassays for the detection and measurement of human antibodies based on EliA solid-phase components, which contain specific antigens for the antibodies to be measured.
The specific antigen for the antibodies to be detected is bound to the EliA solid phase component (EliA Well). The EliA wells are molded cups comparable to excised wells from a microtiter plate. They are made of polystyrene and are coated with the respective antigen.
7
The wells are at the same time a holder of the coupled antigen for convenient automation and a reaction chamber with reaction/washing solution handling based on pipetting to add and aspiration to remove liquids.
If present in the patient's specimen, antibodies to these proteins bind to their specific antigen. After washing away non-bound antibodies, enzyme-labeled antibodies against human IgG antibodies (EliA IqG Conjugate) are added to form an antibodyconjugate complex. After incubation, non-bound conjugate is washed away, and the bound complex is incubated with a Development Solution. After stopping the reaction, the fluorescence in the reaction mixture is measured. The assay directly measures the amount of antibody of interest bound to the antigen coating the EliA well, therefore the higher the value of fluorescent signal detected by the instrument, the higher the amount of antibody bound and detected in the sample tested. To evaluate test results, the response for patient samples is compared directly to the response for calibrators.
Performance Characteristics
-
- Analytical performance:
- a) Precision/Reproducibility:
Precision on Phadia 250
To determine the precision of the assay, the variability was assessed in a study with 21 runs by examining the samples in 252 replicates across 3 lots and 3 instruments over 7 days. The data was calculated against the calibration curve from Day 1. The statistical evaluation was performed by Analysis of Variance. The results are given in the table below.
| Mean
(EliA | Within-Run | | Between-
Run | | Between-
Instrument | | Lot-to-Lot | | Total
Imprecision | |
|---------------|------------|-----|-----------------|-----|------------------------|-----|------------|------|----------------------|------|
| U/mL) | SD | %CV | SD | %CV | SD | %CV | SD | %CV | SD | %CV |
| 5.2 | 0.2 | 3.1 | 0.3 | 5.0 | 0.1 | 1.3 | 0.7 | 14.1 | 0.8 | 15.4 |
| 9.4 | 0.3 | 2.7 | 0.3 | 3.5 | 0.3 | 3.7 | 0.8 | 9.0 | 1.0 | 10.7 |
| 11.1 | 0.2 | 2.2 | 0.2 | 1.6 | 0.3 | 2.4 | 0.2 | 1.7 | 0.4 | 4.1 |
| 105.0 | 2.5 | 2.4 | 2.0 | 1.9 | 1.0 | 0.9 | 0.6 | 0.5 | 3.4 | 3.2 |
| 273.0 | 12.5 | 4.6 | 3.2 | 1.2 | 16.6 | 6.1 | 14.9 | 5.5 | 25.8 | 9.4 |
Within-Lab Imprecision
To determine the within-lab precision of the assay, the variability was assessed in a study with 40 runs by examining the samples in 80 replicates on 1 instrument over 20 days. The data was calculated against the calibration curve from Day 1. The statistical evaluation was performed by Analysis of Variance. The results are qiven in the table below.
8
| Mean
EliA
U/mL | Within-Run | | Between-Run | | Between-Day | | Total
Within-Lab
Imprecision | |
|----------------------|------------|-----|-------------|-----|-------------|-----|------------------------------------|-----|
| | SD | CV% | SD | CV% | SD | CV% | SD | CV% |
| 4.3 | 0.1 | 2.3 | 0.1 | 1.7 | 0.1 | 1.2 | 0.1 | 3.1 |
| 7.3 | 0.2 | 2.7 | 0.0 | 0.0 | 0.2 | 2.2 | 0.3 | 3.5 |
| 9.9 | 0.2 | 2.3 | 0.2 | 1.9 | 0.1 | 0.9 | 0.3 | 3.2 |
| 110 | 3.0 | 2.7 | 1.8 | 1.7 | 1.3 | 1.2 | 3.8 | 3.4 |
Results for within-laboratory study for Phadia 250:
Lot reproducibility study
Three samples were tested in three different "Kits" in order to simulate three different customers using different combinations of EliA SmD -S Well lots and EliA assay reagent lots. The study was performed on one Phadia 250 instrument. Across 7 different days, one run per "Kit" was performed, i.e. a total of 7 runs per "Kit", and a total of 21 runs across three "Kits".
In each run, each of the three samples was tested in 4 replicates, giving a total of 84 replicates per sample over all three "Kits" (3 kits x 7 days x 4 replicates/run = 84 replicates per sample).
| Mean
(EliA U/mL) | Within-Run | | Between-
Run | | Between-Lot | | Total
Imprecision | |
|---------------------|------------|-----|-----------------|-----|-------------|-----|----------------------|-----|
| | SD | CV% | SD | CV% | SD | CV% | SD | CV% |
| 4.3 | 0.1 | 3.1 | 0.1 | 1.8 | 0.1 | 2.2 | 0.2 | 4.2 |
| 7.8 | 0.2 | 2.5 | 0.2 | 2.6 | 0.3 | 3.5 | 0.4 | 5.0 |
| 10.2 | 0.3 | 2.8 | 0.1 | 0.9 | 0.5 | 4.8 | 0.6 | 5.7 |
Results for additional lot reproducibility study for Phadia 250:
Precision on E-module of the Phadia 2500 and Phadia 5000 series:
To determine the precision of the assay on the E-module, which is a representative of the Phadia 2500 and Phadia 5000 series of instruments, the variability was assessed on 5 samples, using one lot of EliA SmDP-S Well.
The variability was assessed in a study with 21 runs by examining the samples in 84 replicates on 3 Phadia 2500E instruments over 7 days. The data was calculated against the calibration curve from Day 1. The statistical evaluation was performed by Analysis of Variance. The results are given in the table below.
9
| Mean EliA | n | Within-
Run | | Between-
Run | | Between-
Instrument | | Total
Imprecision | |
|-----------|----|----------------|-----|-----------------|-----|------------------------|-----|----------------------|------|
| U/mL | | SD | %CV | SD | %CV | SD | %CV | SD | %CV |
| 4.8 | 84 | 0.3 | 6.1 | 0.1 | 2.6 | 0.4 | 8.4 | 0.5 | 10.7 |
| 8.7 | 84 | 0.4 | 4.2 | 0.6 | 7.2 | 0.0 | 0.0 | 0.7 | 8.3 |
| 9.6 | 84 | 0.5 | 5.3 | 0.3 | 2.8 | 0.6 | 6.6 | 0.9 | 8.9 |
| 102 | 84 | 3.7 | 3.6 | 3.7 | 3.6 | 3.4 | 3.4 | 6.2 | 6.1 |
| 256 | 82 | 13.0 | 5.1 | 8.3 | 3.2 | 12.0 | 4.7 | 20.0 | 7.6 |
b) Linearity/Assay Reportable Range:
3 serum samples were diluted in EliA Sample Diluent and tested on Phadia 250 and Phadia 2500E. The ratios of observed/expected values were calculated. The results are summarized below.
Phadia 250
| Dilution Range
| (EliA U/mL) | Slope | Intercept | R2 |
|---|---|---|---|
| 3.2 — 310.8 | 1.00 | 0.58 | 1.00 |
| 2.3 – 230.5 | 1.00 | -0.31 | 1.00 |
| 0.5 — 9.9 | 1.00 | -0.18 | 1.00 |
*Evaluation including 1st dilution step below LoD
Phadia 2500E
| Dilution Range
| (EliA U/mL) | Slope | Intercept | R2 |
|---|---|---|---|
| 3.0 - 329.3 | 1.01 | -2.04 | 1.00 |
| 1.8 – 205.6 | 1.04 | 0.18 | 0.99 |
| 0.6 – 10.4 | 1.02 | 0.00 | 1.00 |
*Evaluation including 1st dilution step below LoD
The claimed linear range for EliA SmDP-S is 0.8 (LoQ) - 310.8 EliA U/mL.
Hook Effect/Over the Range Results:
Not applicable. Results above the upper limit of the measuring range are reported as ">310". No recommendations are made for dilution of samples outside measuring range in the Package Insert.
- c) Traceability, Stability, Expected Values (Controls, Calibrators, or Methods): Traceabilitv:
The IgG calibrators are traceable (via unbroken chain of calibrations) to the International Reference Preparation (IRP) 67/86 of Human Serum Immunoglobulins A, G and M from WHO. New batches of IgG calibrators are compared to a secondary standard (standardized with the IRP) or the IRP directly and adjusted accordingly to meet the correct concentration.
10
The instrument measures specific IgG concentrations in uq/L. By using a conversion factor given by the lot-specific code of the EliA™ test well, the results are automatically converted to EliA U/mL.
Stability:
Data for open and closed real-time stability and on-board stability of EliA IqG reagents and general EliA reagents on Phadia 250 as well as on the E-module of the Phadia 2500 and Phadia 5000 series were cleared with other EliA tests. for example K141375 for the EliA M2 test on Phadia 250 or K151799 for the EliA anti-TG and EliA anti-TPO tests on Phadia 250 and the Phadia 2500 and Phadia 5000 instrument series (E-module).
Shelf-life:
The stability of EliA SmDP-S Wells was evaluated with both, a real-time and accelerated/stress study. The real-time study results support stability of the test under the recommended storage of 2 - 8°C for up to 18 months.
On-board stability:
The on-board stability EliA SmDP-S carriers (containing the antigen coated wells) was tested over 4 weeks using 4 positive and 2 negative samples only on the Phadia 250 instrument. As the storage conditions in the E-module of the Phadia 2500 and Phadia 5000 series are similar to the Phadia 250, the results can also be used for stability claims for these instruments. The onboard stability for the Phadia 250 was determined to be 28 days at 2-8°C.
Open Stability:
Stability after first opening of the foil bag containing the EliA SmDP-S wells was tested and determined to be 9 months at 2-8°C.
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d) Detection limit:
Four blank and four low level samples were measured with two different reagent sets (two lots of antigen wells and conjugate). The four blank samples were created from depleted IgG (IgM, IgA, IgE) sera, each diluted with EliA Sample Diluent. The blank samples and the low-level samples were assayed in six runs using two different sets of test- and method-specific reagents over six different days on each Phadia 250 and Phadia 2500E in 4fold determination. For each instrument type, the total number of combined observations for blank and low-level samples is 96 (48 per reagent set, 12 per sample and reagent set).
The LoD for EliA SmDP-S is 0.7 EliA U/mL, determined consistent with the guidelines in CLSI document EP17-A2 and with proportions of false positives (α) less than 5% and false negatives (β) less than 5%; based on 192 determinations with 96 blank and 96 low-level replicates per instrument type; and LoB of 0.4 EliA U/mL.
| Instrument | LoB
EliA U/mL | LoD
EliA U/mL | LoQ
EliA U/mL |
|-------------------------------------------------------|------------------|------------------|------------------|
| Phadia 250 | 0.3 | 0.5 | 0.7 |
| E-module of the Phadia 2500 and
Phadia 5000 series | 0.4 | 0.7 | 0.8 |
The results are summarized in the table below?
It was decided to use a harmonized LoB of 0.4 EliA U/mL, LoD of 0.7 EliA U/mL, and LoQ of 0.8 EliA U/mL for the immunoassay.
e) Analytical specificity:
Endogenous and Exogenous Interference:
A study was run to investigate whether high concentrations of potentially interfering substances in serum, like bilirubin, hemoglobin, lipemic factor, rheumatoid factor, Ibuprofen, Losartan, Hydroxychloroguine, Azathioprine, Prednisone, Rituximab and Infliximab adversely affect the results of the new device.
Three serum samples (one negative sample, one sample with a concentration within the equivocal range, and one high positive sample) were prediluted in EliA Sample Diluent and spiked with the different interfering substances or blank solution. The samples were tested in triplicates. A calibration curve was run in duplicate. The runs were repeated twice. One batch of EliA antigen wells and one batch of system reagents were used throughout the studies.
The ratio of blank/spiked sample ranged from 0.92 - 1.09 for EliA SmDP-S. No interference was observed up to the concentrations listed in the table below:
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| Potential Interfering
Compound | Concentration in undiluted
sample |
|-----------------------------------|--------------------------------------|
| Bilirubin F | 19.2 mg/dL |
| Bilirubin C | 20.1 mg/dL |
| Hemoglobin | 501 mg/dL |
| Lipemic factor | 1g/dL |
| Rheumatoid factor | 505 IU/mL |
| Ibuprofen | 21.9 mg/dL |
| Losartan | 1.14 mg/dL |
| Hydroxychloroquine | 0.23 mg/dL |
| Azathioprine | 0.26 mg/dL |
| Prednisone | 0.01 mg/dL |
| Rituximab | 109 mg/dL |
| Infliximab | 26.4 mg/dL |
Reference Sera:
Externally defined sera should be measured according to their target values as mentioned by the institution CDC and AMLI.
Using EliA SmDP-S, the results of 22 reference samples (12 CDC, and 10 AMLI) were found in good agreement to the results described by the supplier: All CDC samples were found according to their target. Three AMLI samples which did not contain antibodies to SmD3 but are known to contain SmB,B', SmE and/or SmF could not be detected by the EliA SmDP-S assay.
Carry-Over:
A study was carried out on a Phadia 250 instrument using the test EliA Ro, cleared under K082759. The instruments of the Phadia 2500 and Phadia 5000 series use disposable tips for pipetting samples and a separate pipette for the conjugate, therefore carry-over from samples to conjugate is impossible.
f) Assay Cut-Off:
To define the cut-off, a study was performed using a cohort consisting of 200 clinically defined disease control samples were measured on a Phadia 250 instrument.
The cut-off was set as follows for EliA SmDP-S:
| 10 EliA U/mL | Positive |
In case of equivocal results, it is recommended to retest the patient after 8-12 weeks.
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-
- Comparison Studies:
- a) Method Comparison with Predicate Device:
A total of 628 patient samples with concentrations covering the measuring range were tested.
The samples were analyzed with the EliA SmDP-S and EliA SmDP assay. The test was run in single determination, and values outside the measuring range (n=168) were excluded from statistical analyses. The results are summarized in the tables below:
| N = 460 | EliA SmDP positive:
10 EliA U/mL | EliA SmDP negative:
10 EliA U/mL | 169 | 9 | 178 |
| EliA SmDP-S negative:
10 EliA U/mL | EliA SmDP negative:
10 EliA U/mL | 201 | 7 | 208 |
| EliA SmDP-S negative:
10 EliA U/mL | 19 | 1 | 20 |
| Negative test
≤ 10 EliA U/mL | 85 | 223 | 308 |
| Total | 104 | 224 | 328 |
Sensitivity (95% CI): 18.3% (11.4% - 27.1%) Specificity (95% CI): 99.6% (97.5% - 100%)
The table below shows the results for each clinical subgroup if equivocal results evaluated as negative:
| Diagnostic groups | n | No (%) Positive
EliA SmDP-S |
|---------------------------------|-----|--------------------------------|
| Systemic lupus erythematosus | 104 | 19 (18.3%) |
| Mixed connective tissue disease | 22 | 0 (0%) |
| Sjögren's syndrome | 28 | 0 (0%) |
| Scleroderma | 32 | 0 (0.0%) |
| Polymyositis/Dermatomvositis | 10 | 0 (0%) |
| Rheumatoid arthritis | 52 | 1 (1.9%) |
| Graves' disease | 10 | 0 (0%) |
| Hashimoto's disease | 10 | 0 (0%) |
| Bacterial infections | 30 | 0 (0%) |
| Viral infections | 30 | 0 (0%) |
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- b) Other Clinical Supportive Data: Not applicable.
-
- Clinical Cut-Off: Same as assay cut-off.
-
- Expected Values/Reference Range:
Antibody prevalence in autoimmune patients varies widely depending on disease area. The proportion of sera from a normal population found positive for the antinuclear antibodies covered by the EliA SmDP-S test is below 1%. Expected values may vary depending on the population tested.
The frequency distribution for antinuclear antibodies was investigated in a group of apparently healthy subjects equally distributed by age and gender, using sera from Caucasian, African American, Hispanic and Asian population obtained from a blood bank.
The results are given in the table below:
| Test | n | Median
EliA U/mL | 95th percentile
EliA U/mL | 99th percentile
EliA U/mL |
|-------------|-----|---------------------|------------------------------|------------------------------|
| EliA SmDP-S | 632 | 1.8 | 3.6 | 5.0 |
Proposed Labeling
The labeling is sufficient, and it satisfies the requirements of 21 CFR Part 809.10.
Conclusion
All available data support that both immunoassays, the new device EliA SmDP-S and its predicate device EliA SmDP perform substantially equivalent.
The submitted information in this premarket notification is complete and supports a substantial equivalence decision.