FDA applicant

Urological Associates of Central Jersey P.A.

South Plainfield, NJ1 decision1994–19940 recalls

FDA records 1 decision for Urological Associates of Central Jersey P.A. (South Plainfield, NJ) in 1994: 1 510(k) clearance. All are in product code EYK (Connector, Ureteral Catheter). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, gastroenterology and urology panel, where it files most

How often FDA has decided Urological Associates of Central Jersey P.A.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Urological Associates of Central Jersey P.A. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Urological Associates of Central Jersey P.A. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Urological”

FDA records each applicant name separately; these may or may not be the same firm.

Urological, Inc. 1 Urological Assoc. of Grand Island, P.C. 1

Urological Associates of Central Jersey P.A.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Urological”