Product code ILE— Physical Medicine
OB HELP ARM
- Classification name
- Sling, Arm, Overhead Supported
- Device class
- Class 1
- Regulation
- 21 CFR 890.3475
- Advisory panel
- Physical Medicine
- Total cleared
- 3
- First cleared
- Most recent
Market context for product code ILE
FDA has cleared devices under product code ILE between 1982 and 1983, filed by 3 applicant companies. 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.
Clearances per year
- 1983
- 1982
Top applicants under product code ILE
Recent clearances under product code ILE
Data sourced from openFDA. This site is unofficial and independent of the FDA.