510(k) Report

FDA applicant

Design Technologies, Inc.

Rahway, NJ4 decisions1986–19870 recalls

FDA records 4 decisions for Design Technologies, Inc. (Rahway, NJ) from 1986 to 1987: 4 510(k) clearances. Most are in product codes CCN (Flowmeter, Nonback-Pressure Compensated…) and 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, anesthesiology panel, where it files most

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Design”

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