FDA 510(k), K950944, AMBULATORY (HOLTER) RECORDING SYSTEM

FDA 510(k), K950944, AMBULATORY (HOLTER) RECORDING SYSTEM

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510(K) Number: K950944
Device Name: AMBULATORY (HOLTER) RECORDING SYSTEM
Manufacturer:
Device Classification Name: Computer, Diagnostic, Programmable
Regulation Number: 870.1425
Classification Product Code: DQK
Date Received: 02/17/1995
Decision Date: 06/18/1996
Regulation Medical Specialty: Cardiovascular
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