KZT
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Kit, Disc, Agar Gel Diffusion, Determine Serum Levels Of Gentamicin
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.3450
- Medical specialty
- Clinical Toxicology
- Flags
- Third-party review eligible
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| BIO-BAG TM ENVIRONMENTAL CHAMBER TYPE M (K811067) | Marion Laboratories, Inc. | 1981-04-29 |
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Every clearance here is in the API, with alerts when new ones post.