FDA Product Code OWQ: Reprocessed Intravascular Ultrasound Catheter
FDA product code OWQ covers reprocessed intravascular ultrasound catheters cleared for intracardiac and intraluminal visualization after a validated reprocessing cycle.
IVUS catheters are expensive single-use devices. Reprocessing provides a cost-effective alternative subject to rigorous cleaning, sterilization, and functional performance validation to demonstrate equivalence to the original device.
OWQ devices are Class II medical devices, regulated under 21 CFR 870.1200 and reviewed by the FDA Cardiovascular panel.
Leading manufacturers include Innovative Health, LLC, Sterilmed, Inc. and Abbott Medical.
30
Total
30
Cleared
173d
Avg days
2002
Since
30 devices
Cleared
Aug 18, 2011
REPROCESSED 3D DIAGNOSTIC ULTRASOUND CATHETER
Sterilmed, Inc.
Cardiovascular
219d
Cleared
Oct 21, 2009
REPROCESSED 3D DIAGNOSTIC ULTRASOUND CATHETERS, MODEL SNDSTR10
Ascent Healthcare Solutions
Cardiovascular
75d
Cleared
Mar 29, 2007
REPROCESSED DIAGNOSTIC ULTRASOUND CATHETER
Ascent Healthcare Solutions
Cardiovascular
174d
Cleared
Mar 16, 2005
REPROCESSED DIAGNOSTIC ULTRASOUND CATHETER
Alliance Medical Corp.
Cardiovascular
505d
Cleared
Mar 01, 2005
STERILEMED REPROCESSED IVUS IMAGING CATHETER
Sterilmed, Inc.
Cardiovascular
76d
Cleared
Oct 11, 2002
REPROCESSED IMAGING CATHETERS
Sterilmed, Inc.
Cardiovascular
430d