510(k) Report

FDA applicant

Imdsoft, Ltd.

Rockville, MD1 decision2002–20020 recalls

FDA records 1 decision for Imdsoft, Ltd. (Rockville, MD) in 2002: 1 510(k) clearance. All are in product code MWI (Monitor, Physiological, Patient (Without…). Its devices cite 1 predicate, 0 of them its own earlier devices. 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, cardiovascular panel, where it files most

How often FDA has decided Imdsoft, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Imdsoft, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Imdsoft, Ltd. 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?

  • MWIMonitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 2 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.

  • K012349Metavision Clinical Information SystemImdsoft, Ltd. · 20022cite it

What has FDA decided for it lately?

  • K012349Metavision Clinical Information SystemImdsoft, Ltd. · 2002

The one decision as Imdsoft, Ltd. →