510(k) Report

FDA applicant

Colonial Medical Supply

Las Vegas, NV1 decision2000–20000 recalls

FDA records 1 decision for Colonial Medical Supply (Las Vegas, NV) in 2000: 1 510(k) clearance. All are in product code HIR (Perineometer). 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Colonial Medical Supply since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Colonial Medical Supply 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?

  • HIRPerineometer1decision

Who builds on its devices?

Later devices cite its devices 4 times; 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.

  • K002830Pelvic Muscle TherapyColonial Medical Supply · 20004cite it

What has FDA decided for it lately?

  • K002830Pelvic Muscle TherapyColonial Medical Supply · 2000

The one decision as Colonial Medical Supply →

Other applicant names beginning “Colonial”

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

Colonial Surgical Supply, Inc. 1