FDA 510(k), K050225, HEARTWAVE II CARDIAC DIAGNOSTIC SYSTEM

FDA 510(k), K050225, HEARTWAVE II CARDIAC DIAGNOSTIC SYSTEM

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510(K) Number: K050225
Device Name: HEARTWAVE II CARDIAC DIAGNOSTIC SYSTEM
Manufacturer:
Device Classification Name: Computer, Diagnostic, Programmable
Regulation Number: 870.1425
Classification Product Code: DQK
Date Received: 02/01/2005
Decision Date: 04/07/2005
Regulation Medical Specialty: Cardiovascular
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