Product code IQP— Physical Medicine
HR UNIT
- Classification name
- Rotator, Transverse
- Device class
- Class 1
- Regulation
- 21 CFR 890.3025
- Advisory panel
- Physical Medicine
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code IQP
FDA has cleared device under product code IQP, all in 1979, 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 IQP
Recent clearances under product code IQP
Data sourced from openFDA. This site is unofficial and independent of the FDA.