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FDA 510(k), K042657, VIOPTIX ODISSEY TISSUE OXIMETER TISSUE OXIMETER, MODEL OXY-2
FDA 510(k), K042657, VIOPTIX ODISSEY TISSUE OXIMETER TISSUE OXIMETER, MODEL OXY-2
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$149.00 USD
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510(K) Number: K042657
Device Name: VIOPTIX ODISSEY TISSUE OXIMETER TISSUE OXIMETER, MODEL OXY-2
Manufacturer:
Device Classification Name: Oximeter, Tissue Saturation
Regulation Number: 870.2700
Classification Product Code: MUD
Date Received: 09/28/2004
Decision Date: 01/10/2005
Regulation Medical Specialty: Cardiovascular
Device Name: VIOPTIX ODISSEY TISSUE OXIMETER TISSUE OXIMETER, MODEL OXY-2
Manufacturer:
Device Classification Name: Oximeter, Tissue Saturation
Regulation Number: 870.2700
Classification Product Code: MUD
Date Received: 09/28/2004
Decision Date: 01/10/2005
Regulation Medical Specialty: Cardiovascular
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