FDA applicant

Intertech/Ohio

Fort Myers, FL10 decisions1986–19890 recalls

FDA records 10 decisions for Intertech/Ohio (Fort Myers, FL) from 1986 to 1989: 10 510(k) clearances. Most are in product codes BZA (Connector, Airway (Extension)) and BZO (Set, Tubing And Support, Ventilator (W Harness)). 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 Intertech/Ohio’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Intertech/Ohio since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Intertech/Ohio’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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Other applicant names beginning “Intertech/Ohio”

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

Intertech Resources, Inc. 29

Intertech/Ohio

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Intertech/Ohio”