I-Flow Corp. - FDA 510(k) Cleared Devices
41
Total
41
Cleared
0
Denied
I-Flow Corp. has 41 FDA 510(k) cleared general hospital devices. Based in Irvine, US.
Historical record: 41 cleared submissions from 1988 to 2007.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
41 devices
Cleared
Jan 26, 2007
ON-Q, PAINBUSTER, C-BLOC, SELECT-A-FLOW, ONDEMAND, HOMEPUMP, ECLIPSE,...
General Hospital
65d
Cleared
Nov 21, 2006
ON-Q INTRODUCERS
Anesthesiology
27d
Cleared
Nov 30, 2005
ON-Q CATHETER, ON-ANTIMICROBIAL CATHETER, SOAKER CATHETER, I-FLOW CATHETER
Anesthesiology
183d
Cleared
Sep 09, 2005
I-FLOW ELASTOMERIC PUMP (ON-Q, PAINBUSTER, C-BLOCK, HOMEPUMP, EASYPUMP)
General Hospital
36d
Cleared
Jan 11, 2005
MODIFICATION TO SOAKER CATHETER
Anesthesiology
27d
Cleared
May 24, 2004
I-FLOW ELASTOMERIC PUMP (ON-Q, PAINBUSTER, C-BLOC, HOMEPUMP)
General Hospital
103d
Cleared
Dec 20, 2002
HOMEPUMP, ECLIPSE, C-SERIES, PAINBUSTER, C-BLOC, ON-Q, EASYPUMP, KVO
General Hospital
29d
Cleared
Dec 13, 2002
PARAGON INFUSION SYSTEM WITH BOLUS
General Hospital
25d
Cleared
Oct 18, 2002
I-FLOW ELASTOMERIC PUMP WITH BOLUS
General Hospital
14d
Cleared
Sep 20, 2002
SOAKER CATHETER
General Hospital
22d
Cleared
Mar 26, 2002
I-FLOW ELASTOMERIC PUMP
General Hospital
8d
Cleared
Mar 20, 2002
HOMEPUMP, ECLIPSE, C-SERIES, PAINBUSTER, C-BLOC, ON-Q, EASYPUMP, ONE STEP KVO
General Hospital
19d
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