DeviceClearance

Product code HHF— Obstetrics/Gynecology

EMMETT IUD THREAD RETREIVER

Classification name
Remover, Intrauterine Device, Contraceptive, Hook-Type
Device class
Class 1
Regulation
21 CFR 884.4530
Advisory panel
Obstetrics/Gynecology
Total cleared
6
First cleared
Most recent

Market context for product code HHF

FDA has cleared 6 devices under product code HHF between 1981 and 1994, 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 HHF

Recent clearances under product code HHF

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