510(k) Report

FDA applicant

Vital Medical, Ltd.

Washington, DC1 decision2000–20000 recalls

FDA records 1 decision for Vital Medical, Ltd. (Washington, DC) in 2000: 1 510(k) clearance. All are in product code DPW (Flowmeter, Blood, Cardiovascular). 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 Vital Medical, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vital Medical, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Vital”

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