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

Dilator, Tracheal

21 CFR 874.4420 / Ear, Nose, Throat
FDA source (opens on fda.gov)

KCG is the FDA product code for Dilator, Tracheal, a class I device type, regulated under 21 CFR 874.4420. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and one recall.

Classification record

Product code
KCG
Device name
Dilator, Tracheal
Regulation
21 CFR 874.4420
Device class
Class I
Review panel
Ear, Nose, Throat
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
1

Clearances, product code KCG

By decision year
1 clearance under product code KCG with a decision year between 1982 and 1982, 1982 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KCG by decision year
YearClearances
19821

Applicants with the most clearances

Product code KCG
Applicants holding the most 510(k) clearances under product code KCG
ApplicantClearances
Kelleher Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 85 companies shown, in name order