FDA applicant
Allied Signal, Inc.
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
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.
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) ReportOther applicant names beginning “Allied”
FDA records each applicant name separately; these may or may not be the same firm.