GROUP A STREP, BETA-STREP— 510(k) K884750
Substantially EquivalentAmpcor, Inc.
FDA 510(k) clearance K884750 for GROUP A STREP, BETA-STREP, Substantially Equivalent on 1988-12-22. Applicant: Ampcor, Inc.. Device class: 1.
Clearance details
- Applicant
- Ampcor, Inc.
- Product code
- Code GTZ
- Device class
- Class 1
- Regulation
- 21 CFR 866.3740
- 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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