FDA applicant

Pro-Tech Services, Inc.

Woodinville, WA7 decisions1994–20050 recalls

FDA records 7 decisions for Pro-Tech Services, Inc. (Woodinville, WA) from 1994 to 2005: 7 510(k) clearances. Most are in product codes MNR (Ventilatory Effort Recorder) and GWL (Amplifier, Physiological Signal). 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, anesthesiology panel, where it files most

How often FDA has decided Pro-Tech Services, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pro-Tech Services, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Pro-Tech Services, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?