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

Drape, Pure Latex Sheet, With Self-Retaining Finger Cot

21 CFR 878.4370 / General, Plastic Surgery
FDA source (opens on fda.gov)

EYX is the FDA product code for Drape, Pure Latex Sheet, With Self-Retaining Finger Cot, a class II device type, regulated under 21 CFR 878.4370. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
EYX
Device name
Drape, Pure Latex Sheet, With Self-Retaining Finger Cot
Regulation
21 CFR 878.4370
Device class
Class II
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 EYX

By decision year
1 clearance under product code EYX with a decision year between 1976 and 1976, 1976 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code EYX by decision year
YearClearances
19761

Applicants with the most clearances

Product code EYX
Applicants holding the most 510(k) clearances under product code EYX
ApplicantClearances
V. Mueller O.V. Baxter Healthcare Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code