FDA 510(k), K120151, NEBULAE I

FDA 510(k), K120151, NEBULAE I

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510(K) Number: K120151
Device Name: NEBULAE I
Manufacturer: NORTHGATE TECHNOLOGIES INC.
Device Classification Name: insufflator, laparoscopic
Regulation Number: 884.1730
Classification Product Code: HIF
Date Received: 01/18/2012
Decision Date: 08/17/2012
Regulation Medical Specialty: Obstetrics/Gynecology
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