FDA 510(k), K122381, NEXFIN MODEL 2

FDA 510(k), K122381, NEXFIN MODEL 2

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510(K) Number: K122381
Device Name: NEXFIN MODEL 2
Manufacturer: MARGUERITE THOMLINSON
Device Classification Name: System, Measurement, Blood-Pressure, Non-Invasive
Regulation Number: DXN
Classification Product Code: KXA
Date Received: 08/06/2012
Decision Date: 04/22/2013
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
  • Status: Pending Fast-Track Request
  • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

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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