Product code LTS— Microbiology
DRYSIDE NEISSERIA
- Classification name
- Test Reagents, Neisseria Gonorrhoeae Biochemical
- Device class
- Class 1
- Regulation
- 21 CFR 866.2660
- Advisory panel
- Microbiology
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code LTS
FDA has cleared device under product code LTS, all in 1996, 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 LTS
Recent clearances under product code LTS
Data sourced from openFDA. This site is unofficial and independent of the FDA.