FDA 510(k), K001852, PERIPHERAL ARTERIAL TONOMETER-PAT 1000RD DEVICE

FDA 510(k), K001852, PERIPHERAL ARTERIAL TONOMETER-PAT 1000RD DEVICE

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510(K) Number: K001852
Device Name: PERIPHERAL ARTERIAL TONOMETER-PAT 1000RD DEVICE
Manufacturer: ITAMAR MEDICAL (C.M.) 1997 LTD.
Device Classification Name: Computer, Diagnostic, Programmable
Regulation Number: 870.1425
Classification Product Code: DQK
Date Received: 06/19/2000
Decision Date: 02/21/2001
Regulation Medical Specialty: Cardiovascular
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