510(k) Report

FDA applicant

Ultimate Development Corp.

Tulsa, OK1 decision1994–19940 recalls

FDA records 1 decision for Ultimate Development Corp. (Tulsa, OK) in 1994: 1 510(k) clearance. All are in product code KMI (Monitor, Bed Patient). 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, general hospital panel, where it files most

How often FDA has decided Ultimate Development Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ultimate Development Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ultimate Development Corp. 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?

  • KMIMonitor, Bed Patient1decision

What has FDA decided for it lately?

  • K942770Ultimat-Sensor for Bed Occupancy MonitorUltimate Development Corp. · 1994

The one decision as Ultimate Development Corp. →

Other applicant names beginning “Ultimate”

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

Ultimate Wireforms, Inc. 6Ultimate Concepts, Inc. 3