GMY
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Antisera, Fluorescent, All Types, Escherichia Coli
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 866.3255
- Medical specialty
- Microbiology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| FLUORETEC-M (K770833) | Pfizer, Inc. | 1977-06-08 |
| MICROBIO. PROD. FLUORESCENT ANTIBODY (K770801) | Pfizer Pharmaceuticals | 1977-05-25 |
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Every clearance here is in the API, with alerts when new ones post.