510(k) Report

FDA applicant

Home Medical Services

San Diego, CA4 decisions2000–20020 recalls

FDA records 4 decisions for Home Medical Services (San Diego, CA) from 2000 to 2002: 4 510(k) clearances. Most are in product codes GZJ (Stimulator, Nerve, Transcutaneous, For Pain…) and IPF (Stimulator, Muscle, Powered). No recall is linked to its devices.

FDA’s records also spell it “Home Medical Services, Inc.”.

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

FIG. A — Illustration, neurology panel, where it files most

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

FDA decisions per year

No FDA decision for Home Medical Services since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Home Medical Services’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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