510(k) Report

FDA applicant

Personal Emergency Response System

East Longmeadow, MA1 decision1990–19900 recalls

FDA records 1 decision for Personal Emergency Response System (East Longmeadow, MA) in 1990: 1 510(k) clearance. All are in product code ILQ (System, Communication, Powered). 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, physical medicine panel, where it files most

How often FDA has decided Personal Emergency Response System’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Personal Emergency Response System since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Personal Emergency Response System 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?

  • ILQSystem, Communication, Powered1decision

What has FDA decided for it lately?

  • K904796Medical Alert System, Model 2200 & 4400 V/TPersonal Emergency Response System · 1990

The one decision as Personal Emergency Response System →

Other applicant names beginning “Personal”

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

Personal Products Co. 45Personal Genome Diagnostics, Inc. 3Personal Sound Technologies, Inc. 2Personal Products Co., Div. of Mcneil Ppc, Inc. 2Personal Products Company, Div. of Mcneil-Ppc, Inc. 2Personal Health & Hygiene, Inc. 1Personal Professional Products, Inc. 1Personal Computers For Medicine, Inc. 1Personal Health Institute International 1