510(k) Report

FDA applicant

Behavioral Technology, Inc.

Salt Lake City, UT1 decision2003–20030 recalls

FDA records 1 decision for Behavioral Technology, Inc. (Salt Lake City, UT) in 2003: 1 510(k) clearance. All are in product code LIL (Monitor, Penile Tumescence). 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

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

FDA decisions per year

No FDA decision for Behavioral Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Behavioral Technology, 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?

  • LILMonitor, Penile Tumescence1decision

Whose devices does it build on?

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

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K033126Monarch 21 Penile Plethysmograph SystemBehavioral Technology, Inc. · 20031cites it

What has FDA decided for it lately?

  • K033126Monarch 21 Penile Plethysmograph SystemBehavioral Technology, Inc. · 2003

The one decision as Behavioral Technology, Inc. →