GQQ
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Antisera, Hai, Parainfluenza Virus 1-4
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 866.3400
- Medical specialty
- Microbiology
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| Record | Firm | Date | Builder |
|---|---|---|---|
| GOAT ANTI-INFLUENZA ANTISERA (K780007) | Northeast Biomedical Labs., Inc. | 1978-01-20 | + Add |
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Every clearance here is in the API, with alerts when new ones post.