Product code EYR— General, Plastic Surgery
KEITHLEY CLAMP
- Classification name
- Tourniquet, Gastro-Urology
- Device class
- Class 1
- Regulation
- 21 CFR 878.5900
- Advisory panel
- General, Plastic Surgery
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code EYR
FDA has cleared devices under product code EYR between 1979 and 1981, filed by 2 applicant companies. 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.
Clearances per year
- 1981
- 1979
Top applicants under product code EYR
Recent clearances under product code EYR
Data sourced from openFDA. This site is unofficial and independent of the FDA.