INY
- Product code
- INY
- Device name
- Bed, Patient Rotation, Manual
- Device class
- Class 1
- 21 CFR
- 21 CFR 890.5180
- Medical specialty
- Physical Medicine
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (all years, FDA)
- 1 (all years; only the last 3 years are listed here)
Official FDA classification page: INY
Classification and pathway per current FDA publications. Data from openFDA (CC0).