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

Connector, Ureteral Catheter

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

EYK is the FDA product code for Connector, Ureteral Catheter, a class I device type, regulated under 21 CFR 876.5130. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
EYK
Device name
Connector, Ureteral Catheter
Regulation
21 CFR 876.5130
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
1
Ingested recalls
0

Clearances, product code EYK

By decision year
1 clearance under product code EYK with a decision year between 1994 and 1994, 1994 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code EYK by decision year
YearClearances
19941

Applicants with the most clearances

Product code EYK
Applicants holding the most 510(k) clearances under product code EYK
ApplicantClearances
Urological Associates of Central Jersey P.A.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 20 companies shown, in name order