510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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GAZClass II

Tubing, Noninvasive

21 CFR 880.6740 / General Hospital
FDA source (opens on fda.gov)

GAZ is the FDA product code for Tubing, Noninvasive, a class II device type, regulated under 21 CFR 880.6740. As of , FDA records hold 27 510(k) clearances under this code, the most recent dated , and 14 recalls.

Classification record

Product code
GAZ
Device name
Tubing, Noninvasive
Regulation
21 CFR 880.6740
Device class
Class II
Review panel
General Hospital
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
27
Ingested recalls
14

Clearances, product code GAZ

By decision year
27 clearances under product code GAZ with a decision year between 1976 and 1995, 1983 the highest year at 4.
Show the numbers
510(k) clearances under FDA product code GAZ by decision year
YearClearances
19761
19771
19783
19792
19802
19821
19834
19842
19861
19871
19882
19914
19931
19952

Applicants with the most clearances

Product code GAZ
Applicants holding the most 510(k) clearances under product code GAZ
ApplicantClearances
Adler Instrument Company2
Norton Performance Plastics Corp.2
Abco Dealers, Inc.1
American Hospital Supply1
Baxter Healthcare Corporation1
Burron Medical Products, Inc.1
Core Dynamics, Inc.1
Devon Industries, Inc.1
Endoscopic Technologies, Inc.1
Heyer Schulte Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 177 companies shown, in name order