FDA 510(k), K133879, FORE-SIGHT ELITE ABSOLUTE TISSUE OXIMETER

FDA 510(k), K133879, FORE-SIGHT ELITE ABSOLUTE TISSUE OXIMETER

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510(K) Number: K133879
Device Name: FORE-SIGHT ELITE ABSOLUTE TISSUE OXIMETER
Manufacturer:
Device Classification Name: Oximeter, Tissue Saturation
Regulation Number: 870.2700
Classification Product Code: MUD
Date Received: 12/20/2013
Decision Date: 04/29/2014
Regulation Medical Specialty: Cardiovascular
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