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

Catheter, Upper Urinary Tract

21 CFR 876.5130 / Gastroenterology, Urology
FDA source (opens on fda.gov)

EYC is the FDA product code for Catheter, Upper Urinary Tract, a class II device type, regulated under 21 CFR 876.5130. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
EYC
Device name
Catheter, Upper Urinary Tract
Regulation
21 CFR 876.5130
Device class
Class II
Review panel
Gastroenterology, Urology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
5
Ingested recalls
0

Clearances, product code EYC

By decision year
5 clearances under product code EYC with a decision year between 1989 and 2020, 1989 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code EYC by decision year
YearClearances
19891
19931
20041
20061
20201

Applicants with the most clearances

Product code EYC
Applicants holding the most 510(k) clearances under product code EYC
ApplicantClearances
DeRoyal Industries, Inc.2
Deroyal1
GE Healthcare1
Kosan Far East Ent., Ltd.1

Companies listing this code with FDA

Companies whose registered establishments list this code