FDA PMA
FDA Class 2
30-Day Notice Accepted
🇺🇸 United States
Glucose Oxidase, Glucose
PMA: P990026
·
Supplement: S006
·
Decision Sep 4, 2001
Classifications
1
FEI Numbers
145
Registration Numbers
145
Basic Information
- Device Name
- Glucose Oxidase, Glucose
- Trade Name
- GLUCOWATCH AUTOMATIC GLUCOSE BIOGRAPHER
- PMA Number
- P990026
- Supplement Number
- S006
- Device Class
- FDA Class 2
- Product Code
- CGA
- Generic Name
- GLUCOSE OXIDASE, GLUCOSE
- Regulation Number
- 862.1345
- Medical Specialty
- Clinical Chemistry
- Advisory Committee
- Clinical Chemistry
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- September 4, 2001
- Date Received
- August 15, 2001
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
CHANGE IN SUPPLIER OF GLUCOSE OXIDASE FOR THE AUTOSENSOR TO TOYOBO RESEARCH CENTER CO. LTD.
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| CGA | Glucose Oxidase, Glucose | FDA class 2 | Clinical Chemistry |