Product code ETK— Ear, Nose, Throat
WILSON EUSTACHIAN TUBAL, SONOGRAPH
- Classification name
- Tube, Toynbee Diagnostic
- Device class
- Class 1
- Regulation
- 21 CFR 874.1925
- Advisory panel
- Ear, Nose, Throat
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code ETK
FDA has cleared device under product code ETK, all in 1983, 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 ETK
Recent clearances under product code ETK
Data sourced from openFDA. This site is unofficial and independent of the FDA.