510(k) Report

FDA applicant

Metro Medical Equipment, Inc.

Livonia, MI1 decision2002–20020 recalls

FDA records 1 decision for Metro Medical Equipment, Inc. (Livonia, MI) in 2002: 1 510(k) clearance. All are in product code KPJ (Chamber, Oxygen, Topical, Extremity). 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 and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Metro Medical Equipment, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • KPJChamber, Oxygen, Topical, Extremity1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K020466HEC 1000Metro Medical Equipment, Inc. · 20021cites it

What has FDA decided for it lately?

  • K020466HEC 1000Metro Medical Equipment, Inc. · 2002

The one decision as Metro Medical Equipment, Inc. →

Other applicant names beginning “Metro”

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

Metro Optics of Austin, Inc. 8Metro Optics, Inc. 1Metro. Hospital & Health Center 1Metro-Care 1