Product code INT— Physical Medicine
TABLE, EXAM & MANUPULATION
- Classification name
- Plinth
- Device class
- Class 1
- Regulation
- 21 CFR 890.3520
- Advisory panel
- Physical Medicine
- Total cleared
- 4
- First cleared
- Most recent
Market context for product code INT
FDA has cleared devices under product code INT, all in 1977, 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.
Top applicants under product code INT
Recent clearances under product code INT
Data sourced from openFDA. This site is unofficial and independent of the FDA.