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FDA 510(k), K071168, THE PORTABLE ANSISCOPE
FDA 510(k), K071168, THE PORTABLE ANSISCOPE
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510(K) Number: K071168
Device Name: THE PORTABLE ANSISCOPE
Manufacturer: DYANSYS, INC.
Device Classification Name: electrocardiograph
Regulation Number: 870.2340
Classification Product Code: DPS
Date Received: 04/27/2007
Decision Date: 08/31/2007
Regulation Medical Specialty: Cardiovascular
Device Name: THE PORTABLE ANSISCOPE
Manufacturer: DYANSYS, INC.
Device Classification Name: electrocardiograph
Regulation Number: 870.2340
Classification Product Code: DPS
Date Received: 04/27/2007
Decision Date: 08/31/2007
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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