LQG — Dna-Reagents, Mycoplasma Spp. Class I
FDA product code LQG covers "Dna-Reagents, Mycoplasma Spp.", a Class I medical device regulated under 21 CFR 866.3375. Submissions are reviewed by the Microbiology panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- LQG
- Device Class
- Class I
- Regulation Number
- 866.3375
- Submission Type
- Review Panel
- MI
- Medical Specialty
- Microbiology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K860574 | gen-probe | GEN-PROBE MYCOPLASMA PNEUMONIA RAPID DETECT SYSTEM | July 3, 1986 |