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
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
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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