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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: KXA
Date Received: 06/03/2002
Decision Date: 05/09/2003
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: HYDROCISION GENERAL SURGERY FLUIDJET SYSTEM
Manufacturer: DEBBIE IAMPIETRO
Device Classification Name: Lavage, Jet
Regulation Number: FQH
Classification Product Code: KXA
Date Received: 06/03/2002
Decision Date: 05/09/2003
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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