510(k) Report

FDA applicant

Allied Signal, Inc.

Morristown, NJ2 decisions1988–19920 recalls

FDA records 2 decisions for Allied Signal, Inc. (Morristown, NJ) from 1988 to 1992: 2 510(k) clearances. Most are in product codes LYY (Latex Patient Examination Glove) and LYU (Accessory, Surgical Apparel). 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 Allied Signal, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Allied Signal, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Allied Signal, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Allied”

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