KBY — Set, Filliform, Eustachian Class I
FDA product code KBY covers "Set, Filliform, Eustachian", a Class I medical device regulated under 21 CFR 874.4175. Submissions are reviewed by the Ear, Nose, Throat panel.
Classification Details
- Product Code
- KBY
- Device Class
- Class I
- Regulation Number
- 874.4175
- Submission Type
- Review Panel
- EN
- Medical Specialty
- Ear, Nose, Throat
- Implant
- No