Product code IPS— Physical Medicine

CANE REACHER

Classification name
Cane
Device class
Class 1
Regulation
21 CFR 890.3075
Advisory panel
Physical Medicine
Total cleared
9
First cleared
Most recent

Market context for product code IPS

FDA has cleared 9 devices under product code IPS between 1977 and 1983, filed by 6 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 IPS

Recent clearances under product code IPS

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