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

Drape, Adhesive, Aerosol

21 CFR 878.4380 / General, Plastic Surgery
FDA source (opens on fda.gov)

KGT is the FDA product code for Drape, Adhesive, Aerosol, a class I device type, regulated under 21 CFR 878.4380. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and one recall.

Classification record

Product code
KGT
Device name
Drape, Adhesive, Aerosol
Regulation
21 CFR 878.4380
Device class
Class I
Review panel
General, Plastic Surgery
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 KGT

By decision year
1 clearance under product code KGT with a decision year between 1985 and 1985, 1985 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KGT by decision year
YearClearances
19851

Applicants with the most clearances

Product code KGT
Applicants holding the most 510(k) clearances under product code KGT
ApplicantClearances
Mowbray Co., Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 25 companies shown, in name order