GOI
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Antiserum, Fluorescent, Rabies Virus
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 866.3460
- Medical specialty
- Microbiology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| LIGHT DIAGNOSTICS RABIES DFA REAGENT (K972975) | Light Diagnostics | 1998-12-22 |
| FITC ANTI-RABIES MONOCLONAL GLOBULIN (K820499) | Centocor, Inc. | 1982-04-16 |
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