ILE — Sling, Arm, Overhead Supported Class I
FDA Device Classification
Classification Details
- Product Code
- ILE
- Device Class
- Class I
- Regulation Number
- 890.3475
- Submission Type
- Review Panel
- PM
- Medical Specialty
- Physical Medicine
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K830842 | lic-orthion | OB HELP ARM | April 5, 1983 |
| K823811 | danek medical | OVERHEAD ARM SLINGS | January 14, 1983 |
| K823152 | orthion | OB HELP ARM | November 5, 1982 |