Ascent Healthcare Solutions - FDA 510(k) Cleared Devices
21
Total
21
Cleared
0
Denied
Ascent Healthcare Solutions has 21 FDA 510(k) cleared medical devices. Based in Phoenix, US.
Historical record: 21 cleared submissions from 2006 to 2011. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ascent Healthcare Solutions Filter by specialty or product code using the sidebar.
21 devices
Cleared
Nov 15, 2011
REPROCESSED HAND ACTIVATE SEALER/DIVIDER
General & Plastic Surgery
160d
Cleared
Jul 18, 2011
REPROCESSED ELECTROSURGICAL INSTRUMENT
General & Plastic Surgery
175d
Cleared
Jul 23, 2010
REPROCESSED COMPRESSION SLEEVES
Cardiovascular
113d
Cleared
May 28, 2010
REPROCESSED CS BI-DIECTIONAL DIAGNOSTIC ELECTROPHYSIOLOGY CATHETER
Cardiovascular
120d
Cleared
May 12, 2010
REPROCESSED ULTRASONIC CURVED SHEARS WITH TORQUE WRENCH AND GRIP ASSIST MODEL...
General & Plastic Surgery
76d
Cleared
Mar 19, 2010
REPROCESSED TROCARS, MODEL B5LT AND CB5LT
Gastroenterology & Urology
66d
Cleared
Mar 04, 2010
REPROCESSED ULTRASONIC COAGULATING SHEARS
General & Plastic Surgery
93d
Cleared
Oct 21, 2009
REPROCESSED 3D DIAGNOSTIC ULTRASOUND CATHETERS, MODEL SNDSTR10
Cardiovascular
75d
Cleared
Apr 01, 2009
REPROCESSED ELECTROPHYSIOLOGY CATHETERS
Cardiovascular
51d
Cleared
Sep 16, 2008
REPROCESSED ELECTROPHYSIOLOGY CATHETERS
Cardiovascular
62d
Cleared
Jul 29, 2008
REPROCESSED MASIMO PULSE OXIMETER SENSORS
Anesthesiology
89d
Cleared
Jul 09, 2008
REPROCESSED ELECTROPHYSIOLOGY CATHETERS
Cardiovascular
58d