QUIK-DOT C REACTIVE PROTEIN— 510(k) K892119
Substantially EquivalentAmpcor, Inc.
FDA 510(k) clearance K892119 for QUIK-DOT C REACTIVE PROTEIN, Substantially Equivalent on 1989-04-14. Applicant: Ampcor, Inc.. Device class: 2.
Clearance details
- Applicant
- Ampcor, Inc.
- Product code
- Code DCK
- Device class
- Class 2
- Regulation
- 21 CFR 866.5270
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bridgeport, NJ, US
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