FDA applicant

Intertech Resources, Inc.

Fort Myers, FL29 decisions1987–19961 recall

FDA records 29 decisions for Intertech Resources, Inc. (Fort Myers, FL) from 1987 to 1996: 29 510(k) clearances. Most are in product codes BTM (Ventilator, Emergency, Manual (Resuscitator)) and BYD (Condenser, Heat And Moisture (Artificial Nose)). 1 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 Intertech Resources, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Intertech Resources, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Intertech Resources, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Intertech”

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

Intertech/Ohio 10

Intertech Resources, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Intertech”