LQG
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Dna-Reagents, Mycoplasma Spp.
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 866.3375
- Medical specialty
- Microbiology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| GEN-PROBE MYCOPLASMA PNEUMONIA RAPID DETECT SYSTEM (K860574) | Gen-Probe, Inc. | 1986-07-03 |
Track LQG automatically
Every clearance here is in the API, with alerts when new ones post.