FDA 510(k), K021813, HYDROCISION GENERAL SURGERY FLUIDJET SYSTEM

FDA 510(k), K021813, HYDROCISION GENERAL SURGERY FLUIDJET SYSTEM

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510(K) Number: K021813
Device Name: HYDROCISION GENERAL SURGERY FLUIDJET SYSTEM
Manufacturer: DEBBIE IAMPIETRO
Device Classification Name: Lavage, Jet
Regulation Number: FQH
Classification Product Code: 06/03/2002
Date Received: 05/09/2003
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital

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