Product code JYQ— Ear, Nose, Throat

EAR LOOP

Classification name: Loop, Wire
Device class: Class 1
Regulation: 21 CFR 874.4420
Advisory panel: Ear, Nose, Throat
Total cleared: 2
First cleared: 1987-03-03
Most recent: 1989-01-27

Market context for product code JYQ

FDA has cleared 2 devices under product code JYQ between 1987 and 1989, filed by 2 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

19891 clearance
19871 clearance

Top applicants under product code JYQ

Treace Medical, Inc.1 clearance
Kinetic Medical Products1 clearance

Recent clearances under product code JYQ

K890221 — MICROSURGICAL WIRE LOOPKinetic Medical Products·1989-01-27
K870761 — EAR LOOPTreace Medical, Inc.·1987-03-03

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