FDA 510(k), K081459, CUSA SELECTOR NXT ULTRASONIC TISSUE ABLATION SYSTEM

FDA 510(k), K081459, CUSA SELECTOR NXT ULTRASONIC TISSUE ABLATION SYSTEM

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510(K) Number: K081459
Device Name: CUSA SELECTOR NXT ULTRASONIC TISSUE ABLATION SYSTEM
Manufacturer:
Device Classification Name: Instrument, Ultrasonic Surgical
Regulation Number:
Classification Product Code: LFL
Date Received: 05/23/2008
Decision Date: 08/13/2008
Regulation Medical Specialty:
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