MAGNO ALARM— 510(k) K960849

Substantially Equivalent

Cardiac Assist Devices, Inc.

FDA 510(k) clearance K960849 for MAGNO ALARM, Substantially Equivalent on 1997-03-26. Applicant: Cardiac Assist Devices, Inc.. Device class: 1.

Clearance details

Applicant: Cardiac Assist Devices, Inc.
Product code: Code DTG
Device class: Class 1
Regulation: 21 CFR 870.3690
Advisory panel: Cardiovascular
Date received: 1996-02-20
Decision date: 1997-03-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cleveland, OH, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.