Product code FHM— General, Plastic Surgery
AUTO SUTURE DISP. 30, ETC. & SURG. STAP
- Classification name
- Apparatus, Suturing, Stomach And Intestinal
- 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 FHM
FDA has cleared devices under product code FHM, all in 1980, 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 FHM
Recent clearances under product code FHM
Data sourced from openFDA. This site is unofficial and independent of the FDA.