Product code JYK— General, Plastic Surgery
SHEA'S EAR SPECULUM HOLDER PORT MANNS
- Classification name
- Holder, Ear Speculum
- Device class
- Class 1
- Regulation
- 21 CFR 878.1800
- Advisory panel
- General, Plastic Surgery
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code JYK
FDA has cleared device under product code JYK, all in 1982, 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 JYK
Recent clearances under product code JYK
Data sourced from openFDA. This site is unofficial and independent of the FDA.