FDA 510(k), K180560, Sherlock 3CG+ T ip Confirmation System

FDA 510(k), K180560, Sherlock 3CG+ T ip Confirmation System

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510(K) Number: K180560
Device Name: Sherlock 3CG+ T ip Confirmation System
Manufacturer: C.R. Bard, Inc.
Device Classification Name: catheter, intravascular, therapeutic, long-term greater than 30 days
Regulation Number: 880.5970
Classification Product Code: LJS
Date Received: 03/01/2018
Decision Date: 06/18/2018
Regulation Medical Specialty: General Hospital

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