FDA 510(k), K033696, PERSONAL INJECTOR

FDA 510(k), K033696, PERSONAL INJECTOR

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510(K) Number: K033696
Device Name: PERSONAL INJECTOR
Manufacturer: UNION MEDICO APS
Device Classification Name: introducer, syringe needle
Regulation Number: 880.6920
Classification Product Code: KZH
Date Received: 11/25/2003
Decision Date: 02/16/2005
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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