FDA 510(k) K120151, NEBULAE I, by Northgate Technologies, Inc.

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