IQP
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Rotator, Transverse
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 890.3025
- Medical specialty
- Physical Medicine
- Flags
- GMP exempt
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| HR UNIT (K782148) | Parke-Davis Co. | 1979-01-08 |
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Every clearance here is in the API, with alerts when new ones post.