FDA 510(k), K120301, MEDIGUIDE TECHNOLOGY

FDA 510(k), K120301, MEDIGUIDE TECHNOLOGY

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510(K) Number: K120301
Device Name: MEDIGUIDE TECHNOLOGY
Manufacturer:
Device Classification Name: Computer, Diagnostic, Programmable
Regulation Number: 870.1425
Classification Product Code: DQK
Date Received: 01/31/2012
Decision Date: 02/24/2012
Regulation Medical Specialty: Cardiovascular
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