FQK — Binder, Perineal Class I
FDA product code FQK covers "Binder, Perineal", a Class I medical device regulated under 21 CFR 880.5160. Submissions are reviewed by the General Hospital panel.
Classification Details
- Product Code
- FQK
- Device Class
- Class I
- Regulation Number
- 880.5160
- Submission Type
- Review Panel
- HO
- Medical Specialty
- General Hospital
- Implant
- No