GPM
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Antiserum, Murine Typhus Fever
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 866.3500
- Medical specialty
- Microbiology
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| Record | Firm | Date | Builder |
|---|---|---|---|
| LATEX R. TYPHI (K860557) | Health Research, Inc. | 1986-04-21 | + Add |
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Every clearance here is in the API, with alerts when new ones post.