510(k) Report

FDA applicant

Hospital Products Group

Ny, NY1 decision1985–19850 recalls

FDA records 1 decision for Hospital Products Group (Ny, NY) in 1985: 1 510(k) clearance. All are in product code JOL (Catheter And Tip, Suction). 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 Hospital Products Group’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Hospital Products Group since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Hospital Products Group by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Hospital Products Group’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Hospital”

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