FRW
- Product code
- FRW
- Device name
- Scale, Patient
- Device class
- Class 1
- 21 CFR
- 21 CFR 880.2720
- Medical specialty
- General Hospital
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 48
Official FDA classification page: FRW
Classification and pathway per current FDA publications. Data from openFDA (CC0).