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

Cannula, Nasal, Oxygen

21 CFR 868.5340 / Anesthesiology
FDA source (opens on fda.gov)

CAT is the FDA product code for Cannula, Nasal, Oxygen, a class I device type, regulated under 21 CFR 868.5340. As of , FDA records hold 42 510(k) clearances under this code, the most recent dated , and 6 recalls.

Classification record

Product code
CAT
Device name
Cannula, Nasal, Oxygen
Regulation
21 CFR 868.5340
Device class
Class I
Review panel
Anesthesiology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
42
Ingested recalls
6

Clearances, product code CAT

By decision year
42 clearances under product code CAT with a decision year between 1976 and 2001, 1976 the highest year at 5.
Show the numbers
510(k) clearances under FDA product code CAT by decision year
YearClearances
19765
19773
19781
19793
19801
19812
19821
19831
19845
19853
19865
19881
19892
19914
19922
19931
19941
20011

Applicants with the most clearances

Product code CAT
Applicants holding the most 510(k) clearances under product code CAT
ApplicantClearances
Salter Labs3
Alpine Specialties, Inc.2
Ashai Co., Ltd.2
Hudson Extrusions, Inc.2
Airlife, Inc.1
Andover Medical, Inc.1
B & F Medical Products, Inc.1
Boston Pacific Medical, Inc.1
C.R. Bard Inc1
Chad Therapeutics, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 252 companies shown, in name order