HEARTCARD CARDIAC EVENT MONITOR— 510(k) K944362

Substantially Equivalent

Instromedix, Inc.

FDA 510(k) clearance K944362 for HEARTCARD CARDIAC EVENT MONITOR, Substantially Equivalent on 1995-09-07. Applicant: Instromedix, Inc..

Clearance details

Applicant: Instromedix, Inc.
Product code: Code DXH
Advisory panel: Cardiovascular
Date received: 1994-09-07
Decision date: 1995-09-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hillsboro, OR, US

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