FDA 510(k), K122762, ACCULIS ACCU21 PMTA MICROWAVE TISSUE ABLATION APPLICATOR

FDA 510(k), K122762, ACCULIS ACCU21 PMTA MICROWAVE TISSUE ABLATION APPLICATOR

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510(K) Number: K122762
Device Name: ACCULIS ACCU21 PMTA MICROWAVE TISSUE ABLATION APPLICATOR
Manufacturer:
Device Classification Name: System, Ablation, Microwave And Accessories
Regulation Number: 878.4400
Classification Product Code: NEY
Date Received: 09/10/2012
Decision Date: 11/30/2012
Regulation Medical Specialty: General & Plastic Surgery
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