AMOXICILLIN/CLAVULANIC ACID 2/1
FDA 510(k) clearance K950328 · decided 1995-04-14
Clearance details
- K-number
- K950328
- Device name
- AMOXICILLIN/CLAVULANIC ACID 2/1
- Applicant
- Ab Biodisk North America, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1995-01-19
- Decision date
- 1995-04-14
- Days to decision
- 85 days
- Clearance type
- Traditional
- Product code
- JWY
- Device class
- 2
- Regulation number
- 866.1640
- Medical specialty
- Microbiology
- Advisory committee
- Microbiology
- Location
- S-17136 Solna, Sweden, SE
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
| Record | Firm | Date |
|---|---|---|
| ETEST CLINICAL AMOXI/CLAV 2/1 XL 256 US S30, CATALOG 412240 recall (Z-0818-2023) | Biomerieux Inc | 2023-01-04 |