FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
GLUCOSURE BLOOD GLUCOSE MONITORING SYSTEM
K Number: K002621
·
Decision Jan 22, 2001
Classifications
1
FEI Numbers
131
Registration Numbers
131
Same Product Code
400
Applicant Total
35
Review Days
152
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Basic Information
- Device Name
- GLUCOSURE BLOOD GLUCOSE MONITORING SYSTEM
- K Number
- K002621
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1345
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Apex BioTechnology Corp.
- Date Received
- August 23, 2000
- Decision Date
- January 22, 2001
- Product Code
- CGA
- Advisory Committee
- Clinical Chemistry
- Review Advisory Committee
- CH
- Third Party
- N
Classifications
This FDA 510(k) 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 |
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