Product code INY— Physical Medicine
KINNET
- Classification name
- Bed, Patient Rotation, Manual
- Device class
- Class 1
- Regulation
- 21 CFR 890.5180
- Advisory panel
- Physical Medicine
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code INY
FDA has cleared device under product code INY, all in 1985, filed by 1 applicant company. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Top applicants under product code INY
Recent clearances under product code INY
Data sourced from openFDA. This site is unofficial and independent of the FDA.