DeviceClearance

Product code GAZ— General Hospital

5 - IN - 1 CONNECTOR

Classification name
Tubing, Noninvasive
Device class
Class 2
Regulation
21 CFR 880.6740
Advisory panel
General Hospital
Total cleared
27
First cleared
Most recent

Market context for product code GAZ

FDA has cleared 27 devices under product code GAZ between 1976 and 1995, filed by 25 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 GAZ

Recent clearances under product code GAZ

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