HEARTHWATCH III(TM)— 510(k) K945476

Substantially Equivalent

Instromedix, Inc.

FDA 510(k) clearance K945476 for HEARTHWATCH III(TM), Substantially Equivalent on 1995-11-09. Applicant: Instromedix, Inc..

Clearance details

Applicant: Instromedix, Inc.
Product code: Code DXH
Advisory panel: Cardiovascular
Date received: 1994-11-08
Decision date: 1995-11-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hillsboro, OR, US

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