Product code FHR— General, Plastic Surgery
VISITEC NEEDLE RANGE (GASTERUROLOGY)
- Classification name
- Needle, Gastro-Urology
- Device class
- Class 1
- Regulation
- 21 CFR 878.4800
- Advisory panel
- General, Plastic Surgery
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code FHR
FDA has cleared device under product code FHR, all in 1981, 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 FHR
Recent clearances under product code FHR
Data sourced from openFDA. This site is unofficial and independent of the FDA.