IQP — Rotator, Transverse Class I
FDA product code IQP covers "Rotator, Transverse", a Class I medical device regulated under 21 CFR 890.3025. Submissions are reviewed by the Physical Medicine panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- IQP
- Device Class
- Class I
- Regulation Number
- 890.3025
- Submission Type
- Review Panel
- PM
- Medical Specialty
- Physical Medicine
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K782148 | parke-davis | HR UNIT | January 8, 1979 |