Product code GAC— General, Plastic Surgery
MORGAN ARTHROSCOPIC MENESUS & SYNOVIAL RASP
- Classification name
- Rasp, Surgical, General & Plastic Surgery
- Device class
- Class 1
- Regulation
- 21 CFR 878.4800
- Advisory panel
- General, Plastic Surgery
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code GAC
FDA has cleared devices under product code GAC between 1985 and 1988, 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
- 1988
- 1985
Top applicants under product code GAC
Recent clearances under product code GAC
Data sourced from openFDA. This site is unofficial and independent of the FDA.