GTC
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Antisera, All Types, Klebsiella Spp.
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 866.3340
- Medical specialty
- Microbiology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| SECURET DRAPE & INSTRUMENT RETAINER/INCL (K830276) | Ritmed, Inc. | 1983-03-29 |
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Every clearance here is in the API, with alerts when new ones post.