FRP
- Product code
- FRP
- Device name
- Holder, Infant Position
- Device class
- Class 1
- 21 CFR
- 21 CFR 880.5680
- Medical specialty
- General Hospital
- Marketing pathway
- 510(K)
- Flag
- GMP exempt
- Flag
- Third-party review eligible
- 510(k) clearances (all years, FDA)
- 14 (all years; only the last 3 years are listed here)
Official FDA classification page: FRP
Classification and pathway per current FDA publications. Data from openFDA (CC0).