FDA 510(k), K181667, Thoraguard System

FDA 510(k), K181667, Thoraguard System

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510(K) Number: K181667
Device Name: Thoraguard System
Manufacturer: Centese, Inc.
Device Classification Name: pump, portable, aspiration (manual or powered)
Regulation Number: 878.4780
Classification Product Code: BTA
Date Received: 06/25/2018
Decision Date: 11/29/2018
Regulation Medical Specialty: General & Plastic Surgery

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