Product code KAG— General, Plastic Surgery
CPI PRINTER
- Classification name
- Holder, Speculum, Ent
- Device class
- Class 1
- Regulation
- 21 CFR 878.1800
- Advisory panel
- General, Plastic Surgery
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code KAG
FDA has cleared devices under product code KAG between 1983 and 1984, 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
- 1984
- 1983
Top applicants under product code KAG
Recent clearances under product code KAG
Data sourced from openFDA. This site is unofficial and independent of the FDA.