FDA applicant

Interactive Technologies, Inc.

Washington, DC1 decision1994–19940 recalls

FDA records 1 decision for Interactive Technologies, Inc. (Washington, DC) in 1994: 1 510(k) clearance. All are in product code IQA (System, Environmental Control, Powered). 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, physical medicine panel, where it files most

How often FDA has decided Interactive Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Interactive Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Interactive Technologies, 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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Other applicant names beginning “Interactive”

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

Interactive Consulting, Inc. 1 Interactive Living Systems, Inc. 1

Interactive Technologies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Interactive”