Alliance Medical Corp. - FDA 510(k) Cleared Devices
36
Total
36
Cleared
0
Denied
Alliance Medical Corp. has 36 FDA 510(k) cleared medical devices. Based in Phoenix, US.
Historical record: 36 cleared submissions from 2001 to 2007. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Alliance Medical Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Alliance Medical Corp.
36 devices
Cleared
Mar 19, 2007
REPROCESSED PHACOEMULSIFICATION TIPS
Ophthalmic
371d
Cleared
Aug 31, 2006
REPROCESSED ELECTROPHYSIOLOGY CATHETERS
Cardiovascular
139d
Cleared
Feb 24, 2006
REPROCESSED COMPRESSION SLEEVES
Cardiovascular
49d
Cleared
Feb 17, 2006
ALLIANCE MEDICAL CORPORATION REPROCESSED COMPRESSION SLEEVES
Cardiovascular
36d
Cleared
Feb 13, 2006
REPROCESSED COMPRESSION SLEEVES
Cardiovascular
76d
Cleared
Jan 27, 2006
REPROCESSED EXTERNAL FIXATION DEVICES
Orthopedic
102d
Cleared
Nov 16, 2005
REPROCESSED ELECTROPHYSIOLOGY CATHETER
Cardiovascular
75d
Cleared
Nov 16, 2005
REPROCESSED DAIG LIVEWIRE ELECTROPHYSIOLOGY CATHETERS
Cardiovascular
56d
Cleared
Aug 25, 2005
ALLIANCE MEDICAL CORPORATION REPROCESSED EXTERNAL FIXATION DEVICES
Orthopedic
27d
Cleared
Aug 25, 2005
ALLIANCE MEDICAL CORPORATION REPROCESSED EXTERNAL FIXATION DEVICES
Orthopedic
27d
Cleared
Aug 22, 2005
ALLIANCE MEDICAL CORPORATION REPROCESSED EXTERNAL FIXATION DEVICES
Orthopedic
24d
Cleared
Jun 29, 2005
ALLIANCE MEDICAL CORPORATION REPROCESSED EXTERNAL FIXATION DEVICES
Orthopedic
16d