GWB
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Antisera, Fluorescent, All Types, Streptococcus Pneumoniae
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 866.3740
- Medical specialty
- Microbiology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| CODMAN GAAB NEUROENDOSCOPE (K923555) | Codman & Shurtleff, Inc. | 1993-03-23 |
| PNEUMOTACHOGRAPHY SYSTEM (K760816) | Aftercal, Inc. | 1976-10-29 |
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Every clearance here is in the API, with alerts when new ones post.