GQM
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Antisera, Neutralization, Herpesvirus Hominis
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 866.3305
- Medical specialty
- Microbiology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| COLORGENE FLUORESCENT DNA HYBRIDIZATION TEST / CMV (K875367) | Enzo Biochem, Inc. | 1988-03-28 |
| GOAT ANTI-HERPES SIMPLEX VIRUS TYPE I (K810043) | Vibac Corp. | 1981-05-15 |
| HERPES EIA TEST KIT (K791397) | Microbiological Assoc. | 1979-09-24 |
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