GMA
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Antisera, Fluorescent, Sporothrix Schenekii
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 866.3680
- Medical specialty
- Microbiology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| LA-SPORO ANTIBODY SYSTEM (K802427) | Immuno-Mycologics, Inc. | 1980-10-31 |
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Every clearance here is in the API, with alerts when new ones post.