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

Gas, Collecting Vessel

21 CFR 868.1575 / Anesthesiology
FDA source (opens on fda.gov)

KGK is the FDA product code for Gas, Collecting Vessel, a class I device type, regulated under 21 CFR 868.1575. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
KGK
Device name
Gas, Collecting Vessel
Regulation
21 CFR 868.1575
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
2
Ingested recalls
0

Clearances, product code KGK

By decision year
2 clearances under product code KGK with a decision year between 1977 and 1986, 1977 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KGK by decision year
YearClearances
19771
19861

Applicants with the most clearances

Product code KGK
Applicants holding the most 510(k) clearances under product code KGK
ApplicantClearances
Instrumentation Industries, Incorporated1
Respironics, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code