GSS
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Antisera, Fluorescent, Pseudomonas Aeruginosa
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 866.3415
- Medical specialty
- Microbiology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| TURKEL THORACENTESIS NEEDLE (K921461) | Symbiosis Corp. | 1992-07-30 |
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Every clearance here is in the API, with alerts when new ones post.