FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ALKALINE PHOSPHATASE (ALP)/PNPP
K Number: K761315
·
Decision Feb 24, 1977
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
123
Applicant Total
14
Review Days
63
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Basic Information
- Device Name
- ALKALINE PHOSPHATASE (ALP)/PNPP
- K Number
- K761315
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1050
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Princeton Biomedix
- Date Received
- December 23, 1976
- Decision Date
- February 24, 1977
- Product Code
- CJE
- 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 |
|---|---|---|---|
| CJE | Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes | FDA class 2 | Clinical Chemistry |
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