DeviceClearance

Product code HGH— Obstetrics/Gynecology

DISPOSABLE ENDOSCOPIC CANNULA

Classification name
Cannula, Suction, Uterine
Device class
Class 2
Regulation
21 CFR 884.5070
Advisory panel
Obstetrics/Gynecology
Total cleared
6
First cleared
Most recent

Market context for product code HGH

FDA has cleared 6 devices under product code HGH between 1984 and 2018, filed by 6 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

Top applicants under product code HGH

Recent clearances under product code HGH

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