(122 days)
No
The summary describes a standard automated clinical chemistry analyzer using spectrophotometric and potentiometric methods, robotics, and computer technology for data analysis. There is no mention of AI or ML in the intended use, device description, or performance studies. The "Mentions AI, DNN, or ML" field is explicitly marked as "Not Found".
No
The device is an in vitro diagnostic (IVD) analyzer used for quantitative determination of analytes in body fluids to aid in diagnosis and monitoring, not to directly treat or prevent a disease.
Yes
The device is intended for the quantitative determination of analytes like glucose, creatinine, and urea nitrogen in body fluids, which are used in the diagnosis and treatment of various diseases and conditions. This clearly indicates its role in determining the presence or nature of a disease, which is the definition of a diagnostic device.
No
The device description explicitly states that the TRILOGY Analyzer incorporates robotics and other hardware components for pipetting, diluting, and performing spectrophotometric and potentiometric analysis. It is a physical analyzer, not solely software.
Yes, this device is an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The "Intended Use / Indications for Use" section explicitly states that TRILOGY is for "in vitro determination of analytes in body fluids." It also lists specific analytes (glucose, creatinine, urea nitrogen, sodium, potassium, and chloride) and their intended use in the "diagnosis and treatment" of various conditions.
- Device Description: The "Device Description" further clarifies that the analyzer is intended for "in vitro measurement of various analytes in serum and urine."
- Definition of IVD: An In Vitro Diagnostic device is defined as a medical device intended for use in vitro for the examination of specimens, including blood and tissue samples, derived from the human body, solely or principally for the purpose of providing information concerning a physiological or pathological state, or concerning a congenital abnormality, or to monitor therapeutic measures. The TRILOGY analyzer fits this definition perfectly.
The document clearly indicates that the device is used to analyze body fluids (serum and urine) outside of the body to provide information for diagnosis and treatment, which is the core function of an IVD.
N/A
Intended Use / Indications for Use
TRILOGY is a fully automated, discrete, software-driven, multi-purpose analyzer for spectrophotometric and potentiometric in vitro determination of analytes in body fluids. It is an open system intended for clinical use in a professional setting for use with various chemistry assays that may be adaptable to the analyzer depending on the reagent used to induce a photometric reaction.
TRILOGY is intended for the quantitative determination of glucose, creatinine and urea nitrogen in serum. Glucose measurements are used in the diagnosis and treatment of carbohydrate metabolism disorders including diabetes mellitus, neonatal hypoglycemia and idiopathic hypoglycemia, and of pancreatic islet cell carcinoma. Creatinine measurements are used in the diagnosis and treatment of renal diseases, and in monitoring renal dialysis. Urea nitrogen measurements are used in the diagnosis and treatment of certain renal and metabolic diseases.
TRILOGY includes an optional Ion Selective Electrodes (ISE) module for the measurement of sodium, potassium, and chloride in serum and urine. These measurements are used to monitor electrolyte balance and in the diagnosis and treatment of diseases involving electrolyte imbalance.
Product codes (comma separated list FDA assigned to the subject device)
CGA, CGX, CDQ, CGZ, CEM, JGS, JJE
Device Description
The TRILOGY Analyzer is a fully automated, multi-purpose analyzer used for analysis in clinical chemistry with optional ion selective electrode (ISE) module. The analyzer is intended for the in vitro measurement of various analytes in serum and urine.
The analyzer incorporates robotics, computer and communication technology to perform integrated tasks from pipetting and diluting of patient specimens, assaying specimens in Routine or STAT modes, performing spectrophotometric, and potentiometric modes simultaneously and analyzing data using multiple curve-fitting parameters.
The TRILOGY Analyzer is an open system for multiple disciplines including clinical chemistry and an optional ISE module.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Not Found
Indicated Patient Age Range
Not Found
Intended User / Care Setting
Professional setting
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
Not Found
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
A series of nonclinical studies was conducted to evaluate the performance of the TRILOGY Analyzer and optional ISE module. These studies included method comparison, precision, linearity, interference, and limit of quantitation. The results of all studies demonstrated that the TRILOGY Analyzer performed according to its specifications.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
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.
Roche Diagnostic Systems, Inc. Roche COBAS MIRA® Chemistry System . (K851172), Medica Corp. EasyElectrolytes Analyzer (K000926), JAS Diagnostics, Inc. Glucose Hexokinase (Liquid) Reagent (K011900), JAS Diagnostics, Inc. Creatinine (Single Vial) Reagent (K003247), JAS Diagnostics, Inc. Urea Nitrogen (BUN) Liquid Reagent (K011596)
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.
Not Found
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
§ 862.1345 Glucose test system.
(a)
Identification. A glucose test system is a device intended to measure glucose quantitatively in blood and other body fluids. Glucose measurements are used in the diagnosis and treatment of carbohydrate metabolism disorders including diabetes mellitus, neonatal hypoglycemia, and idiopathic hypoglycemia, and of pancreatic islet cell carcinoma.(b)
Classification. Class II (special controls). The device, when it is solely intended for use as a drink to test glucose tolerance, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 862.9.
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510(k) Summary for TRILOGY Analyzer
1. APPLICANT/SPONSOR
Drew Scientific, Inc. 4230 Shilling Way Dallas, TX 75237
| Contact Person: | Roger Bourrée |
|---|---|
| Telephone: | 214-210-4900 |
Date Prepared: June 19, 2007
2. DEVICE NAME
| Proprietary Name: | TRILOGY Analyzer |
|---|---|
| Common/Usual Name: | Automated Clinical Chemistry Analyzer with Optional Ion |
| Selective Electrode (ISE) Module | |
| Classification Name: | Analyzer, Chemistry (Photometric, Discrete) for Clinical |
| Use |
3. PREDICATE DEVICES
- Roche Diagnostic Systems, Inc. Roche COBAS MIRA® Chemistry System . (K851172)
- Medica Corp. EasyElectrolytes Analyzer (K000926) .
- JAS Diagnostics, Inc. Glucose Hexokinase (Liquid) Reagent (K011900) .
- JAS Diagnostics, Inc. Creatinine (Single Vial) Reagent (K003247) .
- JAS Diagnostics, Inc. Urea Nitrogen (BUN) Liquid Reagent (K011596) .
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4. DEVICE DESCRIPTION
The TRILOGY Analyzer is a fully automated, multi-purpose analyzer used for analysis in clinical chemistry with optional ion selective electrode (ISE) module. The analyzer is intended for the in vitro measurement of various analytes in serum and urine.
The analyzer incorporates robotics, computer and communication technology to perform integrated tasks from pipetting and diluting of patient specimens, assaying specimens in Routine or STAT modes, performing spectrophotometric, and potentiometric modes simultaneously and analyzing data using multiple curve-fitting parameters.
The TRILOGY Analyzer is an open system for multiple disciplines including clinical chemistry and an optional ISE module.
5. INTENDED USE
TRILOGY is a fully automated, discrete, software-driven, multi-purpose analyzer for spectrophotometric and potentiometric in vitro determination of analytes in body fluids. It is an open system intended for clinical use in a professional setting for use with various chemistry assays that may be adaptable to the analyzer depending on the reagent used to induce a photometric reaction.
TRILOG Y is intended for the quantitative determination of glucose, creatinine and urea nitrogen in serum. Glucose measurements are used in the diagnosis and treatment of carbohydrate metabolism disorders including diabetes mellitus, neonatal hypoglycemia and idiopathic hypoglycemia, and of pancreatic islet cell carcinoma. Creatinine measurements are used in the diagnosis and treatment of renal diseases, and in monitoring renal dialysis. Urea nitrogen measurements are used in the diagnosis and treatment of certain renal and metabolic diseases.
TRILOGY includes an optional Ion Selective Electrodes (ISE) module for the measurement of sodium, potassium, and chloride in serum and urine. These measurements are used to monitor electrolyte balance and in the diagnosis and treatment of diseases involving electrolyte imbalance.
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6. TECHNOLOGICAL CHARACTERISTICS AND SUBSTANTIAL EQUIVALENCE
The TRILOGY Analyzer and the predicate device, Roche COBAS MIRA® Chemistry System are fully automated instruments for analysis in clinical chemistry. The intended uses, assay types, data analysis and automation technology of the devices are similar.
The TRILOGY Analyzer with the optional Ion Selective Electrode (ISE) module and the predicate device, Medica Corp. EasyElectrolytes, are automated instruments used for analysis of analytes in serum and urine. The intended use and principle of measurement are the same.
The TRILOGY Analyzer is an open system intended for clinical use for a variety of general chemistry analyses. Three (3) representative clinical chemistry methodologies (Glucose Hexokinase Liquid Reagent, Creatinine (Single Vial) Reagent and Urea Nitrogen (BUN) Liquid Reagent), as cited above, are manufactured by JAS Diagnostics, Inc. All of these reagents are presently 510(k)-cleared under separate submissions and can be utilized without modification on the TRILOGY Analyzer.
7. PERFORMANCE TESTING
A series of nonclinical studies was conducted to evaluate the performance of the TRILOGY Analyzer and optional ISE module. These studies included method comparison, precision, linearity, interference, and limit of quantitation. The results of all studies demonstrated that the TRILOGY Analyzer performed according to its specifications.
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DEPARTMENT OF HEALTH & HUMAN SERVICES
Image /page/3/Picture/1 description: The image shows the logo for the U.S. Department of Health and Human Services. The logo features a stylized eagle with three wing-like shapes. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" is arranged in a circular fashion around the eagle.
Public Health Service
JUL 1 3 2007
Food and Drug Administration 2098 Gaither Road Rockville MD 20850
Drew Scientific, Inc. c/o Ms. Cynthia A. Sinclair, RAC Medical Device Consultants, Inc. 49 Plain Street North Attleboro, MS 02760
Re: K070704
Trade/Device Name: Trilogy Analyzer Regulation Number: 21 CFR 862.1345 Regulation Name: Glucose test system. Regulatory Class: Class II Product Code: CGA, CGX, CDQ, CGZ, CEM, JGS, JJE Dated: June 19, 2007 Received: June 20, 2007
Dear Ms. Sinclair:
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. 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.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such additional controls. Existing major regulations affecting your device can be found in Title 21, Code of Federal Regulations (CFR), Parts 800 to 895. 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 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 Parts 801 and 809); and good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820).
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Page 2 -
This letter will allow you to begin marketing your device as described in your Section 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a logally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market.
If you desire specific information about the application of labeling requirements to your device, or questions on the promotion and advertising of your device, please contact the Office of In Vitro Diagnostic Device Evaluation and Safety at (240) 276-0490. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its tollefree mober (800) 638-2041 or (240) 276-3150 or at its Internet address at http://www.fda.gov/cdrh/industry/support/index.html.
Sincerely yours.
Jean M. Cooper, M.S., D.v.M.
Yean M. Cooper, M.S., D.V.M. Director Division of Chemistry and Toxicology Office of In Vitro Diagnostic Device Evaluation and Safety Center for Devices and Radiological Health
Enclosure
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Indications for Use
510(k) Number (if known): K070704
Device Name: TRILOGY Analyzer
Indications for Use:
TRILOGY is a fully automated, discrete, software-driven, multi-purpose analyzer for spectrophotometric and potentiometric in vitro determination of analytes in body fluids. It is an open system intended for clinical use in a professional setting for use with various chemistry assays that may be adaptable to the analyzer depending on the reagent used to induce a photometric reaction.
TRILOGY is intended for the quantitative determination of glucose, creatinine and urea nitrogen in serum. Glucose measurements are used in the diagnosis and treatment of carbohydrate metabolism disorders including diabetes mellitus, neonatal hypoglycemia and idiopathic hypoglycemia, and of pancreatic islet cell carcinoma. Creatinine measurements are used in the diagnosis and treatment of renal diseases, and in monitoring renal dialysis. Urea nitrogen measurements are used in the diagnosis and treatment of certain renal and metabolic diseases.
TRILOGY includes an optional Ion Selective Electrodes (ISE) module for the measurement of sodium, potassium, and chloride in serum and urine. These measurements are used to montor electrolyte balance and in the diagnosis and treatment of diseases involving electrolyte imbalance.
Prescription Use X (21 CFR 801 Subpart D)
AND/OR
Over-the-Counter Use (21 CFR 801 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of In Vitro Diagnostic Device Evaluation and Safety (OVD)
Division Sign-Off
Office of In Vitro Diagnostic Device Evaluation and Safety
510(k) K070704
June 19, 2007