Cardiomedics Inc

Company: Cardiomedics Inc.
Date: 4/13/01
Product: Counter pulsation devices

No procedures for the development of software used to control devices.
The software used for the operation of the CardiAssist CounterPulsation system was not properly validated. Problems with this software have been identified and corrective measures have been undertaken to replace this software version.

Electro Static Discharge controls in the electronic assembly have not been implemented as specified by written procedures.
FDA District: Los Angeles District

About the author

Amy enjoys researching and writing about developments in medical technology and how that intersects with US law. She received her J.D. from the University of Florida Levin College of Law in 2020 and now works as a Regulatory Associate for SoftwareCPR®, a general-purpose regulatory consulting firm that is recognized globally for their expertise with standards and national regulations pertaining to medical device, mobile medical app, and HealthIT software.

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