510(k) Report

FDA applicant

Intercontinental New Technologies, Inc.

Deer Field, IL1 decision2000–20000 recalls

FDA records 1 decision for Intercontinental New Technologies, Inc. (Deer Field, IL) in 2000: 1 510(k) clearance. All are in product code BWF (Spirometer, Therapeutic (Incentive)). 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 Intercontinental New Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Intercontinental New Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • BWFSpirometer, Therapeutic (Incentive)1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K992256Frolov's Respiration Training Device, FRTD-01Intercontinental New Technologies, Inc. · 2000

The one decision as Intercontinental New Technologies, Inc. →