Product code LQG— Microbiology
GEN-PROBE MYCOPLASMA PNEUMONIA RAPID DETECT SYSTEM
- Classification name
- Dna-Reagents, Mycoplasma Spp.
- Device class
- Class 1
- Regulation
- 21 CFR 866.3375
- Advisory panel
- Microbiology
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code LQG
FDA has cleared device under product code LQG, all in 1986, filed by 1 applicant company. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Top applicants under product code LQG
Recent clearances under product code LQG
Data sourced from openFDA. This site is unofficial and independent of the FDA.