510(k) Report

FDA applicant

Clover Medical Equipment Services, Inc.

Buffalo, NY1 decision1996–19960 recalls

FDA records 1 decision for Clover Medical Equipment Services, Inc. (Buffalo, NY) in 1996: 1 510(k) clearance. All are in product code CAD (Vaporizer, Anesthesia, Non-Heated). 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, anesthesiology panel, where it files most

How often FDA has decided Clover Medical Equipment Services, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Clover Medical Equipment Services, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Clover Medical Equipment Services, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Clover Medical Equipment Services, Inc.’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 “Clover”

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