ETK — Tube, Toynbee Diagnostic Class I
FDA product code ETK covers "Tube, Toynbee Diagnostic", a Class I medical device regulated under 21 CFR 874.1925. Submissions are reviewed by the Ear, Nose, Throat panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- ETK
- Device Class
- Class I
- Regulation Number
- 874.1925
- Submission Type
- Review Panel
- EN
- Medical Specialty
- Ear, Nose, Throat
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K823774 | antares technical associates | WILSON EUSTACHIAN TUBAL, SONOGRAPH | January 17, 1983 |