FDA 510(k) Applications Submitted by I-FLOW CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K063530 11/22/2006 ON-Q, PAINBUSTER, C-BLOC, SELECT-A-FLOW, ONDEMAND, HOMEPUMP, ECLIPSE, C-SERIES, ONE-STEP KVO, EASYPUMP I-FLOW CORP.
K990425 02/11/1999 SIDEKICK INFUSION KIT I-FLOW CORP.
K991513 04/30/1999 HOMEPUMP C-SERIES AND HOMEPUMP C-SERIES ONE-STEP KVO I-FLOW CORP.
K972173 06/09/1997 MEDI-SIS SYRINGE INFUSION SYSTEM I-FLOW CORP.
K992072 06/19/1999 BOLUS ACCESSORY SET I-FLOW CORP.
K982946 08/21/1998 PAINBUSTER INFUSION KIT I-FLOW CORP.
K984063 11/16/1998 PARAGON BASAL/BOLUS ADMINISTRATION SET I-FLOW CORP.
K984146 11/19/1998 PARAGON INFUSION I-FLOW CORP.
K955727 12/18/1995 BAND-IT 20CC DRIVER/ 15 MIN 20CC ADMINISTRATION SET I-FLOW CORP.
K984502 12/18/1998 NERVE BLOCK INFUSION KIT I-FLOW CORP.
K984638 12/31/1998 PARAGON BOLUS ACCESSORY SET I-FLOW CORP.
K980558 02/13/1998 PAINBUSTER INFUSION SYSTEM I-FLOW CORP.
K020251 01/24/2002 PARAGON INFUSION SYSTEM I-FLOW CORP.
K040337 02/11/2004 I-FLOW ELASTOMERIC PUMP (ON-Q, PAINBUSTER, C-BLOC, HOMEPUMP) I-FLOW CORP.
K020660 03/01/2002 HOMEPUMP, ECLIPSE, C-SERIES, PAINBUSTER, C-BLOC, ON-Q, EASYPUMP, ONE STEP KVO I-FLOW CORP.
K020862 03/18/2002 I-FLOW ELASTOMERIC PUMP I-FLOW CORP.
K051401 05/31/2005 ON-Q CATHETER, ON-ANTIMICROBIAL CATHETER, SOAKER CATHETER, I-FLOW CATHETER I-FLOW CORP.
K052117 08/04/2005 I-FLOW ELASTOMERIC PUMP (ON-Q, PAINBUSTER, C-BLOCK, HOMEPUMP, EASYPUMP) I-FLOW CORP.
K022869 08/29/2002 SOAKER CATHETER I-FLOW CORP.
K023318 10/04/2002 I-FLOW ELASTOMERIC PUMP WITH BOLUS I-FLOW CORP.
K063234 10/25/2006 ON-Q INTRODUCERS I-FLOW CORP.
K023827 11/18/2002 PARAGON INFUSION SYSTEM WITH BOLUS I-FLOW CORP.
K023883 11/21/2002 HOMEPUMP, ECLIPSE, C-SERIES, PAINBUSTER, C-BLOC, ON-Q, EASYPUMP, KVO I-FLOW CORP.
K043456 12/15/2004 MODIFICATION TO SOAKER CATHETER I-FLOW CORP.
K984441 12/14/1998 KVO CHECK VALVE ACCESSORY, MODEL EV-0001 I-FLOW CORP.
K991543 05/03/1999 INTRAOP CATHETER I-FLOW CORP.
K994374 12/27/1999 SOAKER CATHETER I-FLOW CORP.


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