FDA 510(k), K870188, NORFOLK MEDICAL BUTTERFLY INFUSION SET

FDA 510(k), K870188, NORFOLK MEDICAL BUTTERFLY INFUSION SET

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510(K) Number: K870188
Device Name: NORFOLK MEDICAL BUTTERFLY INFUSION SET
Manufacturer: NORFOLK MEDICAL PRODUCTS, INC.
Device Classification Name: set, administration, intravascular
Regulation Number: 880.5440
Classification Product Code: FPA
Date Received: 01/16/1987
Decision Date: 02/10/1987
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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