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

Degreaser, Skin, Surgical

21 CFR 878.4730 / General, Plastic Surgery
FDA source (opens on fda.gov)

KOY is the FDA product code for Degreaser, Skin, Surgical, a class I device type, regulated under 21 CFR 878.4730. As of , FDA records hold no 510(k) clearances under this code and 20 recalls.

Classification record

Product code
KOY
Device name
Degreaser, Skin, Surgical
Regulation
21 CFR 878.4730
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
0
Ingested recalls
20

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 15 companies shown, in name order