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

Sheath, Corrugated Rubber, For Nonindwelling Catheter, Sterile

21 CFR 876.5250 / Gastroenterology, Urology
FDA source (opens on fda.gov)

EYT is the FDA product code for Sheath, Corrugated Rubber, For Nonindwelling Catheter, Sterile, a class I device type, regulated under 21 CFR 876.5250. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
EYT
Device name
Sheath, Corrugated Rubber, For Nonindwelling Catheter, Sterile
Regulation
21 CFR 876.5250
Device class
Class I
Review panel
Gastroenterology, Urology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
4
Ingested recalls
0

Clearances, product code EYT

By decision year
4 clearances under product code EYT with a decision year between 1988 and 1994, 1988 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code EYT by decision year
YearClearances
19882
19942

Applicants with the most clearances

Product code EYT
Applicants holding the most 510(k) clearances under product code EYT
ApplicantClearances
Cook Incorporated1
Kendall Healthcare Products Co. Div.Of Tyco Health1
Kit Pak, Inc.1
Sierra Laboratories, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code