FDA 510(k), K872048, TRANSONIC FLOWMETER

FDA 510(k), K872048, TRANSONIC FLOWMETER

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510(K) Number: K872048
Device Name: TRANSONIC FLOWMETER
Manufacturer: SHAWN P CREIGHTON
Device Classification Name: Flowmeter, Blood, Cardiovascular
Regulation Number: DPW
Classification Product Code: KXA
Date Received: 05/28/1987
Decision Date: 06/21/1988
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
  • Status: Pending Fast-Track Request
  • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

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