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

Bandage, Liquid, Skin Protectant

21 CFR 880.5090 / General Hospital
FDA source (opens on fda.gov)

NEC is the FDA product code for Bandage, Liquid, Skin Protectant, a class I device type, regulated under 21 CFR 880.5090. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and 6 recalls.

Classification record

Product code
NEC
Device name
Bandage, Liquid, Skin Protectant
Regulation
21 CFR 880.5090
Device class
Class I
Review panel
General Hospital
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
3
Ingested recalls
6

Clearances, product code NEC

By decision year
3 clearances under product code NEC with a decision year between 1986 and 1997, 1986 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code NEC by decision year
YearClearances
19862
19971

Applicants with the most clearances

Product code NEC
Applicants holding the most 510(k) clearances under product code NEC
ApplicantClearances
Aplicare, Inc.2
Medlogic Global Limited1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 140 companies shown, in name order