KBR — Needle, Tonsil Suturing Class I
FDA product code KBR covers "Needle, Tonsil Suturing", a Class I medical device regulated under 21 CFR 874.4420. Submissions are reviewed by the Ear, Nose, Throat panel.
Classification Details
- Product Code
- KBR
- Device Class
- Class I
- Regulation Number
- 874.4420
- Submission Type
- Review Panel
- EN
- Medical Specialty
- Ear, Nose, Throat
- Implant
- No