FDA 510(k), K830009, OXYMIZER

FDA 510(k), K830009, OXYMIZER

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510(K) Number: K830009
Device Name: OXYMIZER
Manufacturer:
Device Classification Name: Conserver, Oxygen
Regulation Number: NFB
Classification Product Code: KXA
Date Received: 01/03/1983
Decision Date: 04/02/1983
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
  • 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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