FDA applicant

First Medical Devices Corp.

Bellevue, WA7 decisions1986–19900 recalls

FDA records 7 decisions for First Medical Devices Corp. (Bellevue, WA) from 1986 to 1990: 7 510(k) clearances. Most are in product codes LDD (Dc-Defibrillator, Low-Energy, (Including…) and MKJ (Automated External Defibrillators (Non-Wearable)). 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 First Medical Devices Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for First Medical Devices Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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First Medical Devices Corp.

Which product codes does it file in?

What has FDA decided for it lately?