510(k) Report

FDA applicant

Morgan Associates, Inc.

Walker, MI2 decisions1983–19880 recalls

FDA records 2 decisions for Morgan Associates, Inc. (Walker, MI) from 1983 to 1988: 2 510(k) clearances. Most are in product codes CCK (Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase) and GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). 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 Morgan Associates, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Morgan Associates, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Morgan Associates, Inc. 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?

  • CCKAnalyzer, Gas, Carbon-Dioxide, Gaseous-Phase1decision
  • GZJStimulator, Nerve, Transcutaneous, For Pain Relief1decision

What has FDA decided for it lately?

  • K884032Morgan Transcutaneous Electrical Nerve StimulatorMorgan Associates, Inc. · 1988
  • K832005JP-2 Respiratory Monitoring SystemMorgan Associates, Inc. · 1983

All 2 as Morgan Associates, Inc. →

Other applicant names beginning “Morgan”

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

Morgan Scientific, Inc. 6Morgan Medical Co. 2Morgan Technology, Inc. 1