(142 days)
Not Found
No
The device description explicitly states it is a "reusable mechanical, non-electronic ambulatory infusion pump that does not require batteries or any electrical source." It uses a spring for pressure and relies on the physical properties of tubing for flow control. There is no mention of any computational or data-driven components that would suggest AI/ML.
Yes
The device is used to infuse therapeutic substances (Immune Globulin Solutions) into the body, which is a form of therapy.
No
Explanation: The device is an infusion system designed for delivering medication, not for diagnosing medical conditions. Its purpose is to administer specified immune globulin solutions subcutaneously.
No
The device description explicitly states that the SCIg60 Infusion System consists of a mechanical, non-electronic infusion pump (SCIg60 Infuser), flow control extension sets, and patient administration sets. It is a hardware-based system.
Based on the provided text, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use clearly states the device is for the "subcutaneous infusion of Hizentra, Immune Globulin Subcutaneous (Human), 20% Liquid... Gammagard Liquid, Immune Globulin Infusion (Human) 10%... and Cuvitru Immune Globulin Infusion (Human) 20%". This describes a device used to administer medication into the body, not to perform tests on samples taken from the body.
- Device Description: The description details a "mechanical, non-electronic ambulatory infusion pump" that uses a spring to deliver fluid. This is consistent with a drug delivery device, not a diagnostic device.
- Lack of IVD Characteristics: The text does not mention any of the typical characteristics of an IVD, such as:
- Analyzing biological samples (blood, urine, tissue, etc.)
- Detecting or measuring substances in samples
- Providing information for diagnosis, monitoring, or screening
Therefore, the SCIg60 Infusion System is a drug delivery device, not an In Vitro Diagnostic device.
N/A
Intended Use / Indications for Use
The SCIg60 Infusion System is intended for use in the home or hospital environment for the subcutaneous infusion of Hizentra, Immune Globulin Subcutaneous (Human), 20% Liquid (manufactured by CSL Behring), Gammagard Liquid, Immune Globulin Infusion (Human) 10% (manufactured by Baxalta), and Cuvitru Immune Globulin Infusion (Human) 20% (manufactured by Baxalta) with the BD 60 ml syringe (model no. 309653).
Product codes (comma separated list FDA assigned to the subject device)
PKP
Device Description
The EMED SCIg60 Infusion System consists of the SCIg60 Infuser, the Infuset™ flow control extension set and SUB-Q patient administration set. The SCIg60 Infuser must be used with the BD 60 ml syringe (model no. 309653). The Infuset™ flow control extension sets and SUB-Q patient administration sets are also manufactured by EMED Technologies.
The SCIg60 Infuser is a reusable mechanical. non-electronic ambulatory infusion pump that does not require batteries or any electrical source. The EMED SCIg60 Infuser uses a spring as a source of pressure for the subcutaneous infusion of indicated human plasma-derived immunoglobulin solutions.
The Infuset™ flow control extension sets are assembled from standard luer lock components and specified lengths of PVC microbore tubing. The length and diameter of the tubing results in predetermined flow rates when used with the SCIg60 Infuser, and include slide-clamps for stopping the flow of fluid. The SCIg60 Infuser user manual includes information to guide users in the selection of Infuset™ flow control extension sets and SUB-Q patient administration sets users to achieve the desired infusion rates.
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
home or hospital environment
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 safety assurance case for the SCI260 Infusion System was provided, as recommended by the FDA guidance document, Infusion Pumps Total Product Life Cycle. The stated top-level claim of the assurance case is: The SCIg60 Infusion System is adequately safe for its intended use. The safety assurance case defined the device system. including the indications for use, patient types. users, use conditions, environments of use, and list of specific devices covered by the assurance case. The supporting sub-claims of the assurance case included the following:
- Device design is adequately verified and validated
- Device associated risks are completely identified and adequately mitigated
- Device is adequately reliable to ensure safety over device use life
The assurance case included mitigations of risks related to the following hazards:
- Operational Hazards
- Hardware Hazards
- Mechanical Hazards
- Environmental Hazards
- Biological and Chemical Hazards
- Use Hazards
The assurance case identified and claimed mitigation of the following device system level hazards:
- Infusion Delivery Error
- Traumatic Injury
- Incorrect Therapy
- Biological or Chemical Contamination
The following testing and evaluations were covered in the Safety Assurance Case:
- Infusion flow rate testing with SCIg60 Infusion System and indicated human plasma-derived immunoglobulin solutions.
- Infusion flow rate testing with combinations of SCIg60 Infuser. Infuset 100 extension sets, and SUB-Q patient administration sets with simulated test fluid for the indicated human plasma-derived immunoglobulin solutions.
- Validation of simulated test fluids.
- Influence of elevation on flow rate for indicated human plasma-derived immunoglobulin solutions.
- Human factors validation of the SCIg60 Infusion System.
- Compatibility of each indicated human plasma-based immunoglobulin solution with the SCIg60 Infusion System related to adverse impact to either the SCIg60 Infusion System or the indicated fluids. The drug-device compatibility data referenced in K142319 for Hizentra was leveraged for Gammagard and Cuvitru after a comparison of factors that could impact the results of drug-device compatibility (e.g., pH and concentration).
- Reliability, biocompatibility, sterility and shelf life data were incorporated by reference to data from K142319.
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.
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
§ 880.5725 Infusion pump.
(a)
Identification. An infusion pump is a device used in a health care facility to pump fluids into a patient in a controlled manner. The device may use a piston pump, a roller pump, or a peristaltic pump and may be powered electrically or mechanically. The device may also operate using a constant force to propel the fluid through a narrow tube which determines the flow rate. The device may include means to detect a fault condition, such as air in, or blockage of, the infusion line and to activate an alarm.(b)
Classification. Class II (performance standards).
0
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Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002
December 1, 2016
EMED Technologies Corporation Peter Kollings Director Regulatory Affairs and Quality Assurance 1264 Hawks Flight Ct, Ste. 200 El Dorado Hills, California 95762
Re: K161906
Trade/Device Name: SCIg60 Infusion System Regulation Number: 21 CFR 880.5725 Regulation Name: Infusion Pump Regulatory Class: II Product Code: PKP Dated: October 28, 2016 Received: October 31, 2016
Dear Peter Kollings:
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. 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.
1
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 Part 801): medical device reporting of medical devicerelated adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (OS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address
http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm. 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
http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.
You may obtain other general information on your responsibilities under the Act from the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address
http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.
Sincerely,
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Tina Kiang, Ph.D. Acting Director Division of Anesthesiology. General Hospital, Respiratory, Infection Control, and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
2
Indications for Use
510(k) Number (if known) K161906
Device Name SCIg60 Infusion System
Indications for Use (Describe)
The SCIg60 Infusion System is intended for use in the home or hospital environment for the subcutaneous infusion of Hizentra, Immune Globulin Subcutaneous (Human), 20% Liquid (manufactured by CSL Behring), Gammagard Liquid, Immune Globulin Infusion (Human) 10% (manufactured by Baxalta), and Cuvitru Immune Globulin Infusion (Human) 20% (manufactured by Baxalta) with the BD 60 ml syringe (model no. 309653).
Type of Use (Select one or both, as applicable)
2 Prescription Use (Part 21 CFR 801 Subpart D)
_ Over-The-Counter Use (21 CFR 801 Subpart C)
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3
510(k) Summary
K161906
Summary Prepared: December 1, 2016
General Information
Classification Class II Trade Name SCIg60 Infusion System Common Name: Infusion Pump Classification Name and Reference: Pump, Infusion Regulation: 21 CFR §880.5725 Product Code: PKP (immunoglobulin g (IgG) infusion system)
Submitter Peter Kollings EMED Technologies Corporation 1264 Hawks Flight Ct El Dorado Hills, Ca Tel: 916.932.0071 Fax: 916.932.0074
General
This 510k submission for premarket clearance of the SCIg60 Infusion System is intended to expand the indications for use of the K142319 predicate to include infusion of the following human plasmaderived immunoglobulin solutions:
- -Gammagard Liquid, Immune Globulin Infusion (Human) 10% (manufactured by Baxalta),
- -Cuvitru Immune Globulin Infusion (Human) 20% (manufactured by Baxalta)
Bevond the expanded indications for use and associated updates to labeling, the SCIg60 Infusion System that is the subject of this submission is identical to that of the predicate in terms of principle of action, design, materials, functionality, and general performance.
Indications for Use
The SCIg60 Infusion System is intended for use in the home or hospital environment for the subcutaneous infusion of Hizentra, Immune Globulin Subcutaneous (Human), 20% Liquid (manufactured by CSL Behring). Gammagard Liquid, Immune Globulin Infusion (Human) 10% (manufactured by Baxalta), and Cuvitru Immune Globulin Infusion (Human) 20% (manufactured by Baxalta) with the BD 60 ml syringe (model no. 309653).
Comparison of Indications for Use of Subject and Predicate devices
The proposed indications for use of the SCIg60 Infusion System are identical to that of the predicate with the exception that infusion of Gammagard and Cuvitru are included.
The additional biological products being added to the SCIg60 Infusion System labeling have similar physicochemical characteristics to Hizentra with regard to composition, purity, presence
4
of trace contaminants, formulation and function. Any differences do not raise new issues of safety or effectiveness or alter the intended therapeutic effect because the principle of action. labeling, and overall design the SCIg60 Infusion System account for and accommodate such variations in human-plasma derived immunoglobulin solutions.
Primary Predicate Device(s)
K142319, SCIg60 Infusion System
Device Description
The EMED SCIg60 Infusion System consists of the SCIg60 Infuser, the Infuset™ flow control extension set and SUB-Q patient administration set. The SCIg60 Infuser must be used with the BD 60 ml syringe (model no. 309653). The Infuset™ flow control extension sets and SUB-Q patient administration sets are also manufactured by EMED Technologies.
The SCIg60 Infuser is a reusable mechanical. non-electronic ambulatory infusion pump that does not require batteries or any electrical source. The EMED SCIg60 Infuser uses a spring as a source of pressure for the subcutaneous infusion of indicated human plasma-derived immunoglobulin solutions.
The Infuset™ flow control extension sets are assembled from standard luer lock components and specified lengths of PVC microbore tubing. The length and diameter of the tubing results in predetermined flow rates when used with the SCIg60 Infuser, and include slide-clamps for stopping the flow of fluid. The SCIg60 Infuser user manual includes information to guide users in the selection of Infuset™ flow control extension sets and SUB-Q patient administration sets users to achieve the desired infusion rates.
SCIg60 Infusion System should be used in accordance with its directions for use.
Technological Characteristics
The overall principle of action for the SCIg60 Infusion System consists of a constant pressure source acting upon a syringe filled with fluid, with the flow rate of that fluid being regulated by PVC tubing with fixed fluid path dimensions (i.e. tubing length and inner diameter). The flow control properties of the tubing follows the Poiseuille equation in that pressure, length of fluid path, diameter of fluid path, and viscosity of a fluid in a system directly influence resultant flow rates of that fluid.
The SCIg60 Infuser, Infuset 101 flow control extension sets, and SUB-Q patient administration sets are identical to those presented in K142319.
The total flow rate range of the SCIg60 Infusion System has been adjusted from 12 - 52 ml/hr to 11 – 145 ml/hr to reflect the manufacturer-recommended total flow rates of the additional indicated immunoglobulin biologics. The increased upper limit of the total flow rate range does not represent a change in SCIg60 Infusion System design or performance, but instead reflects the expanded indications for use: the Prescribing Information for several of the proposed immunoglobulin solutions allow for greater total and per-site flow rates than Hizentra (the indicated biologic for the predicate). Additionally, manufacturers of proposed immunoglobulin solutions may also allow for use of more than 4 needles at once, thereby allowing for further increases in the upper limit of the total flow range performance range when compared with the predicate.
5
It is noted that the SCIg60 Infusion System instructions for use include only those combinations of Infuset and SUB-Q sets that provide flow rate performance in line with indicated immunoglobulin manufacturer recommendations. Combinations that allow for flow rates that exceed manufacturer recommendations are not provided. Therefore, the increased upper limit of the total flow rate range is acceptable in terms of clinical use as well as compliance with flow rate recommendations provided by immunoglobulin solution manufacturers.
Summary of Performance Testing
A safety assurance case for the SCI260 Infusion System was provided, as recommended by the FDA guidance document, Infusion Pumps Total Product Life Cycle. The stated top-level claim of the assurance case is:
The SCIg60 Infusion System is adequately safe for its intended use.
The safety assurance case defined the device system. including the indications for use, patient types. users, use conditions, environments of use, and list of specific devices covered by the assurance case. The supporting sub-claims of the assurance case included the following:
- Device design is adequately verified and validated
- Device associated risks are completely identified and adequately mitigated
- . Device is adequately reliable to ensure safety over device use life
The assurance case included mitigations of risks related to the following hazards:
- Operational Hazards ●
- Hardware Hazards
- Mechanical Hazards ●
- Environmental Hazards
- . Biological and Chemical Hazards
- Use Hazards
The assurance case identified and claimed mitigation of the following device system level hazards:
- . Infusion Delivery Error
- Traumatic Injury
- Incorrect Therapy
- Biological or Chemical Contamination
The following testing and evaluations were covered in the Safety Assurance Case:
- Infusion flow rate testing with SCIg60 Infusion System and indicated human plasma-derived . immunoglobulin solutions.
- Infusion flow rate testing with combinations of SCIg60 Infuser. Infuset 100 extension sets, and . SUB-Q patient administration sets with simulated test fluid for the indicated human plasmaderived immunoglobulin solutions.
- Validation of simulated test fluids. .
6
- Influence of elevation on flow rate for indicated human plasma-derived immunoglobulin solutions.
- Human factors validation of the SCIg60 Infusion System. ●
- . Compatibility of each indicated human plasma-based immunoglobulin solution with the SCIg60 Infusion System related to adverse impact to either the SCIg60 Infusion System or the indicated fluids. The drug-device compatibility data referenced in K142319 for Hizentra was leveraged for Gammagard and Cuvitru after a comparison of factors that could impact the results of drug-device compatibility (e.g., pH and concentration).
- Reliability, biocompatibility, sterility and shelf life data were incorporated by reference to ● data from K142319.
The SCIg60 Infusion System includes directions for the selection of Infuset™ flow control extension sets and SUB-Q patient administration set combinations in order to achieve desired infusion rates for each of the indicated human plasma-derived immunoglobulin solutions, in accordance with the following tables:
Hizentra
First Infusion of Hizentra
| Needle
Gauge | Number
of needles | Total
Flow
Rate
(ml/hr) | Approx. Per
Site Flow
Rate
(ml/hr) | Infuset™
Reorder
Number | SUB-Q Set |
|-----------------|----------------------|----------------------------------|---------------------------------------------|-------------------------------|-------------|
| 24 | 1 | 12 | 12 | FP-0010008 | SUB-109-G24 |
| | 4 | 39 | 10 | FP-0010009 | SUB-409-G24 |
| 27 | 2 | 25 | 13 | FP-0010005 | SUB-260 |
| | 4 | 47 | 12 | FP-0010004 | SUB-410 |
Standard Infusions of Hizentra
| Needle
Gauge | Number
of needles | Total
Flow Rate
(ml/hr) | Approx. Per
Site Flow
Rate
(ml/hr) | Infuset™
Reorder
Number | SUB-Q Set |
|-----------------|----------------------|-------------------------------|---------------------------------------------|-------------------------------|-------------|
| 24 | 1 | 12 | 12 | FP-0010008 | SUB-109-G24 |
| | 1 | 16 | 16 | FP-0010007 | SUB-109-G24 |
| | 2 | 26 | 13 | FP-0010010 | SUB-209-G24 |
| | 2 | 35 | 18 | FP-0010009 | SUB-209-G24 |
| | 3 | 39 | 10 | FP-0010009 | SUB-309-G24 |
| | 3 | 51 | 17 | FP-0010005 | SUB-309-G24 |
| | 4 | 39 | 10 | FP-0010009 | SUB-409-G24 |
| | 4 | 52 | 13 | FP-0010005 | SUB-409-G24 |
| 27 | 1 | 14 | 14 | FP-0010009 | SUB-109-G27 |
7
| Needle
Gauge | Number
of needles | Total
Flow Rate
(ml/hr) | Approx. Per
Site Flow
Rate
(ml/hr) | Infuset™
Reorder
Number | SUB-Q Set |
|-----------------|----------------------|-------------------------------|---------------------------------------------|-------------------------------|-------------|
| | | 17 | 17 | FP-0010004 | SUB-109-G27 |
| | 2 | 25 | 13 | FP-0010005 | SUB-260 |
| | | 30 | 16 | FP-0010004 | SUB-260 |
| | 3 | 43 | 14 | FP-0010004 | SUB-320 |
| | 4 | 47 | 12 | FP-0010004 | SUB-410 |
Gammagard
Initial Infusion of Gammagard (patients weighing less than 40kg)
| Needle
Gauge | Number of
needles | Total Flow
Rate
(ml/hr) | Approx.
Per Site
Flow Rate
(ml/hr) | Infuset™
Reorder
Number | SUB-Q Set |
|-----------------|----------------------|-------------------------------|---------------------------------------------|-------------------------------|-------------|
| 24 | 2 | 25 | 12 | FP-0010014 | SUB-209-G24 |
| | 4 | 29 | 7 | FP-0010011 | SUB-409-G24 |
| | 5 | 63 | 13 | FP-0010008 | SUB-512-G24 |
| 27 | 1 | 13 | 13 | FP-0010013 | SUB-109-G27 |
| | 2 | 25 | 12 | FP-0010011 | SUB-260 |
| | 5 | 57 | 11 | FP-0010008 | SUB-509 |
8
| Needle
Gauge | Number of
needles | Total Flow
Rate
(ml/hr) | Approx.
Per Site
Flow Rate
(ml/hr) | InfusetTM
Reorder
Number | SUB-Q Set |
|-----------------|----------------------|-------------------------------|---------------------------------------------|--------------------------------|-------------|
| 24 | 1 | 15 | 15 | FP-0010013 | SUB-109-G24 |
| | 2 | 25 | 12 | FP-0010014 | SUB-209-G24 |
| | 4 | 29 | 15 | FP-0010011 | SUB-209-G24 |
| | 5 | 29 | 7 | FP-0010011 | SUB-409-G24 |
| | 6 | 63 | 13 | FP-0010008 | SUB-512-G24 |
| | | 95 | 16 | FP-0010007 | SUB-612-G24 |
| 27 | 1 | 13 | 13 | FP-0010013 | SUB-109-G27 |
| | 2 | 25 | 12 | FP-0010011 | SUB-260 |
| | 3 | 51 | 17 | FP-0010008 | SUB-320 |
| | 5 | 57 | 11 | FP-0010008 | SUB-509 |
| | 6 | 88 | 15 | FP-0010007 | SUB-609 |
Maintenance Infusions of Gammagard (patients weighing less than 40kg)
Initial Infusion of Gammagard (patients weighing 40kg or more)
| Needle
Gauge | Number of
needles | Total Flow
Rate
(ml/hr) | Approx.
Per Site
Flow Rate
(ml/hr) | InfusetTM
Reorder
Number | SUB-Q Set |
|-----------------|----------------------|-------------------------------|---------------------------------------------|--------------------------------|-------------|
| 24 | 1 | 15 | 15 | FP-0010013 | SUB-109-G24 |
| | 2 | 25 | 12 | FP-0010014 | SUB-209-G24 |
| | 2 | 29 | 15 | FP-0010011 | SUB-209-G24 |
| | 4 | 29 | 7 | FP-0010011 | SUB-409-G24 |
| | 5 | 63 | 13 | FP-0010008 | SUB-512-G24 |
| | 6 | 95 | 16 | FP-0010007 | SUB-612-G24 |
| 27 | 1 | 13 | 13 | FP-0010013 | SUB-109-G27 |
| | 2 | 25 | 12 | FP-0010011 | SUB-260 |
| | 3 | 51 | 17 | FP-0010008 | SUB-320 |
| | 5 | 57 | 11 | FP-0010008 | SUB-509 |
| | 6 | 88 | 15 | FP-0010007 | SUB-609 |
9
| Needle
Gauge | Number of
needles | Total Flow
Rate
(ml/hr) | Approx.
Per Site
Flow Rate
(ml/hr) | Infuset™
Reorder
Number | SUB-Q Set |
|-----------------|----------------------|-------------------------------|---------------------------------------------|-------------------------------|-------------|
| 24 | 1 | 15 | 15 | FP-0010013 | SUB-109-G24 |
| | 1 | 24 | 24 | FP-0010014 | SUB-109-G24 |
| | 2 | 25 | 12 | FP-0010014 | SUB-209-G24 |
| | 2 | 29 | 15 | FP-0010011 | SUB-209-G24 |
| | 3 | 59 | 20 | FP-0010008 | SUB-309-G24 |
| | 4 | 29 | 7 | FP-0010011 | SUB-409-G24 |
| | 4 | 94 | 24 | FP-0010007 | SUB-409-G24 |
| | 5 | 63 | 13 | FP-0010008 | SUB-512-G24 |
| | 6 | 95 | 16 | FP-0010007 | SUB-612-G24 |
| 27 | 1 | 13 | 13 | FP-0010013 | SUB-109-G27 |
| | 1 | 21 | 21 | FP-0010014 | SUB-109-G27 |
| | 1 | 23 | 23 | FP-0010011 | SUB-109-G27 |
| | 2 | 25 | 12 | FP-0010011 | SUB-260 |
| | 2 | 47 | 24 | FP-0010008 | SUB-260 |
| | 3 | 51 | 17 | FP-0010008 | SUB-320 |
| | 3 | 71 | 24 | FP-0010007 | SUB-320 |
| | 4 | 80 | 20 | FP-0010007 | SUB-410 |
| | 5 | 57 | 11 | FP-0010008 | SUB-509 |
| 5 | 121 | 24 | FP-0010010 | SUB-509 | |
| 6 | 88 | 15 | FP-0010007 | SUB-609 | |
Maintenance Infusions of Gammagard (patients weighing 40kg or more)
Cuvitru
First 2 Infusions of Cuvitru
| Needle
Gauge | Number of
needles | Total Flow
Rate
(ml/hr) | Approx.
Per Site
Flow Rate
(ml/hr) | InfusetTM
Reorder
Number | SUB-Q Set |
|-----------------|----------------------|-------------------------------|---------------------------------------------|--------------------------------|-------------|
| 24 | 1 | 11 | 11 | FP-0010008 | SUB-109-G24 |
| | | 14 | 14 | FP-0010007 | SUB-109-G24 |
| | | 17 | 17 | FP-0010010 | SUB-109-G24 |
| | 2 | 20 | 10 | FP-0010010 | SUB-209-G24 |
| | | 32 | 16 | FP-0010009 | SUB-209-G24 |
| | 3 | 35 | 12 | FP-0010009 | SUB-309-G24 |
| | | 45 | 15 | FP-0010005 | SUB-309-G24 |
| | 4 | 49 | 12 | FP-0010005 | SUB-409-G24 |
10
| Needle
Gauge | Number of
needles | Total Flow
Rate
(ml/hr) | Approx. Per
Site Flow
Rate
(ml/hr) | Infuset™
Reorder
Number | SUB-Q Set |
|-----------------|----------------------|-------------------------------|---------------------------------------------|-------------------------------|-------------|
| 24 | 1 | 11 | 11 | FP-0010008 | SUB-109-G24 |
| | | 14 | 14 | FP-0010007 | SUB-109-G24 |
| | | 17 | 17 | FP-0010010 | SUB-109-G24 |
| | | 31 | 31 | FP-0010005 | SUB-109-G24 |
| | 2 | 20 | 10 | FP-0010010 | SUB-209-G24 |
| | | 32 | 16 | FP-0010009 | SUB-209-G24 |
| | | 42 | 21 | FP-0010005 | SUB-209-G24 |
| | | 94 | 47 | FP-0010004 | SUB-209-G24 |
| | 3 | 35 | 12 | FP-0010009 | SUB-309-G24 |
| | | 45 | 15 | FP-0010005 | SUB-309-G24 |
| | | 118 | 39 | FP-0010004 | SUB-309-G24 |
| | 4 | 49 | 12 | FP-0010005 | SUB-409-G24 |
| | | 145 | 36 | FP-0010004 | SUB-409-G24 |
Subsequent Infusions of Cuvitru
Summary of Substantial Equivalence
The performance data demonstrates that the EMED Technologies Corporation SCIg60 Infusion System is substantially equivalent to the predicate device and provides infusion rates consistent with the FDA approved human plasma-derived immunoglobulin labeling, when used as directed.