FDA applicant
Pro-Tech, Inc.
FDA records 7 decisions for Pro-Tech, Inc. (Woodinville, WA) from 1992 to 1995: 7 510(k) clearances. Most are in product codes BZG (Spirometer, Diagnostic) and MNR (Ventilatory Effort Recorder). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Pro-Tech, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Pro-Tech, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Pro-Tech, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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