FDA 510(k), K102520, BD NEXIVA CLOSED IV CATHETER SYSTEM

FDA 510(k), K102520, BD NEXIVA CLOSED IV CATHETER SYSTEM

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510(K) Number: K102520
Device Name: BD NEXIVA CLOSED IV CATHETER SYSTEM
Manufacturer: JUSTICE ALDER
Device Classification Name: Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Regulation Number: FOZ
Classification Product Code: KXA
Date Received: 09/02/2010
Decision Date: 01/06/2011
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
  • 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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