PMA supplement

P150009 S004: AngelMed Guardian System

FDA PMA supplement · 30-Day Notice · CJ Healthtech Holdings, LLC

Key facts

Original PMA P150009
Supplement number S004
Supplement type 30-Day Notice
Reason for the supplement Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name AngelMed Guardian System
Generic name Acute coronary syndrome event detector
Applicant CJ Healthtech Holdings, LLC
Product code QBI
Received date Dec 1, 2020
Decision date Dec 22, 2020

At a glance

  • No Expedited review granted
  • No Approval order on file
  • No Summary of safety and effectiveness on file

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About PMA supplements

A PMA supplement asks FDA to approve a change to a device that already holds a premarket approval: a new indication, a design or labeling change, a manufacturing site or process change.

Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date:

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