Advanced Infusion, Inc. is one of 21582 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Advanced Infusion, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ALPHA INFUSION PUMP, MODEL A200, A450, STA CATH ATTACHABLE INFISION CATHETER, MODEL STA20, POLYURETHANE INFUSION CATHETER, ALPHA CATH, MODEL PAC20, AND POLYURETHANE INFUSION CATHETER, MULTI DRIP, MODEL PMD20-6
6
Total
6
Cleared
0
Denied
Advanced Infusion, Inc. has 6 FDA 510(k) cleared medical devices. Based in Tempe, US.
Historical record: 6 cleared submissions from 1999 to 2008. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Advanced Infusion, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Entela, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Advanced Infusion, Inc.
6 devices
Cleared
Feb 19, 2008
ALPHA INFUSION PUMP, MODEL A200, A450
General Hospital
259d
Cleared
Oct 18, 2006
STA CATH ATTACHABLE INFISION CATHETER, MODEL STA20
General Hospital
127d
Cleared
Jul 03, 2006
POLYURETHANE INFUSION CATHETER, ALPHA CATH, MODEL PAC20, AND POLYURETHANE...
General Hospital
49d
Cleared
Aug 31, 2004
MULTI-DRIP INFUSION CATHETER
General Hospital
12d
Cleared
Aug 12, 2002
ALPHA INFUSION PUMP AND CATHETERS
General Hospital
59d
Cleared
Oct 27, 1999
ALPHA INFUSION PUMP
General Hospital
89d