DeviceClearance

Product code KTC— Physical Medicine

ABCO PLASTIC UTENSILS

Classification name
Bath, Sitz, Nonpowered
Device class
Class 1
Regulation
21 CFR 890.5125
Advisory panel
Physical Medicine
Total cleared
7
First cleared
Most recent

Market context for product code KTC

FDA has cleared 7 devices under product code KTC between 1980 and 1991, filed by 7 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 KTC

Recent clearances under product code KTC

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