KBM — Dissector, Tonsil Class I
FDA product code KBM covers "Dissector, Tonsil", a Class I medical device regulated under 21 CFR 874.4420. 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
- KBM
- Device Class
- Class I
- Regulation Number
- 874.4420
- Submission Type
- Review Panel
- EN
- Medical Specialty
- Ear, Nose, Throat
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K940903 | medical insights | TONSIL SPONGE, GAUZE DISSECTOR, CYLINDRICAL SPONGES | April 14, 1994 |