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FDA 510(k), K011625, VASOCOR VASCULAR DIAGNOSTIC CENTER (MODEL 300)
FDA 510(k), K011625, VASOCOR VASCULAR DIAGNOSTIC CENTER (MODEL 300)
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510(K) Number: K011625
Device Name: VASOCOR VASCULAR DIAGNOSTIC CENTER (MODEL 300)
Manufacturer: VASOCOR, INC.
Device Classification Name: system, measurement, blood-pressure, non-invasive
Regulation Number: 870.1130
Classification Product Code: DXN
Date Received: 05/25/2001
Decision Date: 01/23/2002
Regulation Medical Specialty: Cardiovascular
Device Name: VASOCOR VASCULAR DIAGNOSTIC CENTER (MODEL 300)
Manufacturer: VASOCOR, INC.
Device Classification Name: system, measurement, blood-pressure, non-invasive
Regulation Number: 870.1130
Classification Product Code: DXN
Date Received: 05/25/2001
Decision Date: 01/23/2002
Regulation Medical Specialty: Cardiovascular
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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