• FDA 510(k) records for MobileRay Pulse SE Digital Imaging System K191503
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FDA 510(k) K120640, INSUFLOW SYNERGY PORT, by Lexion Medical, LLC

FDA 510(k) K120640, INSUFLOW SYNERGY PORT, by Lexion Medical, LLC

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510(K) Number: K120640
Device Name: INSUFLOW SYNERGY PORT
Manufacturer: Lexion Medical, LLC
Device Classification Name: insufflator, laparoscopic
Regulation Number: 884.1730
Classification Product Code: HIF
Date Received: 03/02/2012
Decision Date: 07/18/2012
Regulation Medical Specialty: Obstetrics/Gynecology
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