Product code IQK— Physical Medicine

CERVICAL COLLAR

Classification name
Orthosis, Cervical
Device class
Class 1
Regulation
21 CFR 890.3490
Advisory panel
Physical Medicine
Total cleared
27
First cleared
Most recent

Market context for product code IQK

FDA has cleared 27 devices under product code IQK between 1977 and 1993, filed by 22 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 IQK

Recent clearances under product code IQK

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