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FDA 510(k) K133821, EMPRINT ABLATION SYSTEM, by Covidien, LLC

FDA 510(k) K133821, EMPRINT ABLATION SYSTEM, by Covidien, LLC

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510(K) Number: K133821
Device Name: EMPRINT ABLATION SYSTEM
Manufacturer: Covidien, LLC
Device Classification Name: system, ablation, microwave and accessories
Regulation Number: 878.4400
Classification Product Code: NEY
Date Received: 12/16/2013
Decision Date: 04/28/2014
Regulation Medical Specialty: General & Plastic Surgery
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