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

Cream, Gloving, Surgeon'S

21 CFR 878.4470 / General, Plastic Surgery
FDA source (opens on fda.gov)

KGQ is the FDA product code for Cream, Gloving, Surgeon'S, a class I device type, regulated under 21 CFR 878.4470. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
KGQ
Device name
Cream, Gloving, Surgeon'S
Regulation
21 CFR 878.4470
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
0

Clearances, product code KGQ

By decision year
1 clearance under product code KGQ with a decision year between 1991 and 1991, 1991 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KGQ by decision year
YearClearances
19911

Applicants with the most clearances

Product code KGQ
Applicants holding the most 510(k) clearances under product code KGQ
ApplicantClearances
Guardian Angel Products, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code