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

Cylinder, Compressed Gas, And Valve

21 CFR 868.2700 / Anesthesiology
FDA source (opens on fda.gov)

ECX is the FDA product code for Cylinder, Compressed Gas, And Valve, a class I device type, regulated under 21 CFR 868.2700. As of , FDA records hold 13 510(k) clearances under this code, the most recent dated , and 15 recalls.

Classification record

Product code
ECX
Device name
Cylinder, Compressed Gas, And Valve
Regulation
21 CFR 868.2700
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
13
Ingested recalls
18

Clearances, product code ECX

By decision year
13 clearances under product code ECX with a decision year between 1977 and 2017, 2006 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code ECX by decision year
YearClearances
19771
20041
20062
20071
20111
20142
20152
20162
20171

Applicants with the most clearances

Product code ECX
Applicants holding the most 510(k) clearances under product code ECX
ApplicantClearances
Air Liquide Healthcare America3
Aga-Linde Health Care1
Air Liquide Healthcare1
Essex Industries, Inc1
Linde Gas North America, LLC1
Linde Gas Therapeutics1
Pattient Safety Innovations, LLP1
Praxair Distribution, Incorporated.1
Praxair Healthcare Services1
Star Dental Mfg. Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 17 companies shown, in name order