Product code KNM— Physical Medicine
AUTONOM
- Classification name
- Device, Pressure Applying
- Device class
- Class 1
- Regulation
- 21 CFR 890.5765
- Advisory panel
- Physical Medicine
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code KNM
FDA has cleared devices under product code KNM between 1978 and 1981, 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.
Clearances per year
- 1981
- 1978
Top applicants under product code KNM
Recent clearances under product code KNM
Data sourced from openFDA. This site is unofficial and independent of the FDA.