ALKALINE PHOSPHATASE REAGENT
FDA 510(k) clearance K792551 · decided 1980-01-29
Clearance details
- K-number
- K792551
- Device name
- ALKALINE PHOSPHATASE REAGENT
- Applicant
- Electrophoresis Corp. of America
- Decision
- Substantially Equivalent
- Date received
- 1979-12-10
- Decision date
- 1980-01-29
- Days to decision
- 50 days
- Clearance type
- Traditional
- Product code
- CJH
- Device class
- 2
- Regulation number
- 862.1050
- Medical specialty
- Clinical Chemistry
- Advisory committee
- Clinical Chemistry
- Location
- Walker, MI, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.