DeviceClearance

Product code JZF— Ear, Nose, Throat

EXMOOR TYMPANOCENTESIS KIT (TK/1)

Classification name
Tube, Ear Suction
Device class
Class 1
Regulation
21 CFR 874.4420
Advisory panel
Ear, Nose, Throat
Total cleared
5
First cleared
Most recent

Market context for product code JZF

FDA has cleared 5 devices under product code JZF between 1982 and 1998, filed by 5 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 JZF

Recent clearances under product code JZF

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