RPR TEST FOR SYPHILIS IN SERUM OR PLASMA— 510(k) K880477
Substantially EquivalentAmpcor, Inc.
FDA 510(k) clearance K880477 for RPR TEST FOR SYPHILIS IN SERUM OR PLASMA, Substantially Equivalent on 1988-03-30. Applicant: Ampcor, Inc.. Device class: 2.
Clearance details
- Applicant
- Ampcor, Inc.
- Product code
- Code GMQ
- Device class
- Class 2
- Regulation
- 21 CFR 866.3820
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bridgeport, NJ, US
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More clearances from Ampcor, Inc.
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