Product code IOD— Physical Medicine

ANKLE WEIGHTS

Classification name
Components, Exercise
Device class
Class 1
Regulation
21 CFR 890.5350
Advisory panel
Physical Medicine
Total cleared
11
First cleared
Most recent

Market context for product code IOD

FDA has cleared 11 devices under product code IOD between 1976 and 1983, filed by 5 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.

Clearances per year

Top applicants under product code IOD

Recent clearances under product code IOD

Data sourced from openFDA. This site is unofficial and independent of the FDA.