FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
OPTIONAL TOTAL CA-MODULE FOR IL 504/508
K Number: K812872
·
Decision Oct 26, 1981
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
4
Applicant Total
321
Review Days
12
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Basic Information
- Device Name
- OPTIONAL TOTAL CA-MODULE FOR IL 504/508
- K Number
- K812872
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1100
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Instrumentation Laboratory CO
- Date Received
- October 14, 1981
- Decision Date
- October 26, 1981
- Product Code
- CIS
- 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 |
|---|---|---|---|
| CIS | Hydrazone Colorimetry, Ast/Sgot | FDA class 2 | Clinical Chemistry |
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