FDA 510(k), K012044, BI-PHASIC INFILTRATOR

FDA 510(k), K012044, BI-PHASIC INFILTRATOR

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510(K) Number: K012044
Device Name: BI-PHASIC INFILTRATOR
Manufacturer: RELIANCE MEDICAL CORP.
Device Classification Name: pump, infusion
Regulation Number: 880.5725
Classification Product Code: FRN
Date Received: 06/29/2001
Decision Date: 08/28/2001
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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