JWW
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Antigen, Cf, B. Dermatitidis
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 866.3060
- Medical specialty
- Microbiology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| IMMUNODIFFUSSION REAGENTS/SEROLOGICAL (K802128) | Nolan Biological Laboratories, Inc. | 1980-09-26 |
| BLASTOMYCES/ANTIGEN FOR IMMUNODIFUSION (K792683) | Meridian Diagnostics, Inc. | 1980-01-23 |
| BLASTOMYCES DERMATITIDIS, ANTIGEN (K792680) | Meridian Diagnostics, Inc. | 1980-01-17 |
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Every clearance here is in the API, with alerts when new ones post.