MCC
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Dna-Probe, Haemophilus Spp.
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 866.3300
- Medical specialty
- Microbiology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| ACCUPROBE LISTERIA MONOCYTOGENES CULTURE CONFIRMA. (K901397) | Gen-Probe, Inc. | 1990-06-20 |
| ACCUPROBE HAEOMPHILUS INFLUENZAE CULTURE (K897079) | Gen-Probe, Inc. | 1990-03-08 |
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Every clearance here is in the API, with alerts when new ones post.