Product code GBP— General, Plastic Surgery
CATHETER, MULTIPLE LUMEN
- Classification name
- Catheter, Multiple Lumen
- Device class
- Class 1
- Regulation
- 21 CFR 878.4200
- Advisory panel
- General, Plastic Surgery
- Total cleared
- 3
- First cleared
- Most recent
Market context for product code GBP
FDA has cleared devices under product code GBP between 1982 and 1985, filed by 3 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
- 1985
- 1982
Top applicants under product code GBP
Recent clearances under product code GBP
Data sourced from openFDA. This site is unofficial and independent of the FDA.