FDA applicant

Urological Assoc. of Grand Island, P.C.

Grand Island, NE1 decision1989–19890 recalls

FDA records 1 decision for Urological Assoc. of Grand Island, P.C. (Grand Island, NE) in 1989: 1 510(k) clearance. All are in product code FMF (Syringe, Piston). 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, general hospital panel, where it files most

How often FDA has decided Urological Assoc. of Grand Island, P.C.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Urological Assoc. of Grand Island, P.C. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Urological Assoc. of Grand Island, P.C. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Urological Assoc. of Grand Island, P.C.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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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 Associates of Central Jersey P.A. 1

Urological Assoc. of Grand Island, P.C.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Urological”