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FDA 510(k), K031327, VERICOR
FDA 510(k), K031327, VERICOR
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510(K) Number: K031327
Device Name: VERICOR
Manufacturer: T. WHIT ATHEY
Device Classification Name: System, Measurement, Blood-Pressure, Non-Invasive
Regulation Number: DXN
Classification Product Code: KXA
Date Received: 04/25/2003
Decision Date: 05/12/2004
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: VERICOR
Manufacturer: T. WHIT ATHEY
Device Classification Name: System, Measurement, Blood-Pressure, Non-Invasive
Regulation Number: DXN
Classification Product Code: KXA
Date Received: 04/25/2003
Decision Date: 05/12/2004
Decision: Substantially Equivalent (SESE)
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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