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

Protector, Wound, Plastic

21 CFR 878.4014 / General, Plastic Surgery
FDA source (opens on fda.gov)

EYF is the FDA product code for Protector, Wound, Plastic, a class I device type, regulated under 21 CFR 878.4014. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
EYF
Device name
Protector, Wound, Plastic
Regulation
21 CFR 878.4014
Device class
Class I
Review panel
General, Plastic Surgery
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
5
Ingested recalls
0

Clearances, product code EYF

By decision year
5 clearances under product code EYF with a decision year between 1983 and 1992, 1991 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code EYF by decision year
YearClearances
19831
19901
19912
19921

Applicants with the most clearances

Product code EYF
Applicants holding the most 510(k) clearances under product code EYF
ApplicantClearances
Autovage1
Central Plastic, Inc.1
MEDLINE INDUSTRIES, LP - Northfield1
David F. Trungale1
Harding Medical Devices1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code EYF.