Product code INE— Physical Medicine
ACCULITE-PPL 5
- Classification name
- Sling, Overhead Suspension, Wheelchair
- Device class
- Class 1
- Regulation
- 21 CFR 890.3910
- Advisory panel
- Physical Medicine
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code INE
FDA has cleared device under product code INE, all in 1989, 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 INE
Recent clearances under product code INE
Data sourced from openFDA. This site is unofficial and independent of the FDA.