Product code INQ— Physical Medicine

POWERMATIC EXAMINATION TABLE

Classification name
Table, Powered
Device class
Class 1
Regulation
21 CFR 890.3760
Advisory panel
Physical Medicine
Total cleared
102
First cleared
Most recent

Market context for product code INQ

FDA has cleared 102 devices under product code INQ between 1977 and 1996, filed by 35 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

last 15 years

Top applicants under product code INQ

Recent clearances under product code INQ

1–100 of 102

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