FQK
- Product code
- FQK
- Device name
- Binder, Perineal
- Device class
- Class 1
- 21 CFR
- 21 CFR 880.5160
- Medical specialty
- General Hospital
- Marketing pathway
- 510(K) Exempt
- Flag
- GMP exempt
Official FDA classification page: FQK
Classification and pathway per current FDA publications. Data from openFDA (CC0).