FDA 510(k), K100744, CERTUS 140 MICROWAVE ABLATION SYSTEM AND ACCESSORIES, MODEL CERTUS 140

FDA 510(k), K100744, CERTUS 140 MICROWAVE ABLATION SYSTEM AND ACCESSORIES, MODEL CERTUS 140

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510(K) Number: K100744
Device Name: CERTUS 140 MICROWAVE ABLATION SYSTEM AND ACCESSORIES, MODEL CERTUS 140
Manufacturer: NEUWAVE MEDICAL, INC
Device Classification Name: system, ablation, microwave and accessories
Regulation Number: 878.4400
Classification Product Code: NEY
Date Received: 03/16/2010
Decision Date: 10/22/2010
Regulation Medical Specialty: General & Plastic Surgery

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