Cleared Traditional

K063076 - REPROCESSED DIAGNOSTIC ULTRASOUND CATHETER

K063076 is an FDA 510(k) clearance for REPROCESSED DIAGNOSTIC ULTRASOUND CATHETER, manufactured by Ascent Healthcare Solutions. The device is a Class 2 Cardiovascular device with product code OWQ cleared through the Traditional 510(k) pathway after a 174-day FDA review.

K063076 · Ascent Healthcare Solutions · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 2007
Decision
174d
Days
Class 2
Risk

K063076 is an FDA 510(k) clearance for the REPROCESSED DIAGNOSTIC ULTRASOUND CATHETER. Classified as Reprocessed Intravascular Ultrasound Catheter (product code OWQ), Class II - Special Controls.

Submitted by Ascent Healthcare Solutions (Phoenix, US). The FDA issued a Cleared decision on March 29, 2007 after a review of 174 days - an extended review cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1200 - the FDA cardiovascular device oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Cardiovascular review framework, consistent with the majority of Class II 510(k) submissions.

View all Ascent Healthcare Solutions devices

FDA 510(k) Submission Details - K063076

510(k) Number K063076 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 06, 2006
Decision Date March 29, 2007
Days to Decision 174 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
49d slower than avg
Panel avg: 125d · This submission: 174d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

OWQ Device Classification - Class 2, Special Controls

Product Code OWQ Reprocessed Intravascular Ultrasound Catheter
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1200
Definition For Intracardiac And Intraluminal Visualization Of Cardiovascular Anatomy And Physiology.
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Cardiovascular devices follow this clearance model.

Regulatory Peers - OWQ Reprocessed Intravascular Ultrasound Catheter

All 27
Devices cleared under the same product code (OWQ) and FDA review panel - the closest regulatory comparables to K063076.
SoundStar eco 8F 3D Diagnostic eco Ultrasound Catheters, SoundStar eco 8F G 3D Diagnostic eco Ultrasound Catheters
K161700 · Sterilmed, Inc. · Nov 2016
Reprocessed Diagnostic Ultrasound Catheter
K153090 · Innovative Health, LLC · Mar 2016
REPROCESSED 3D DIAGNOSTIC ULTRASOUND CATHETER
K110076 · Sterilmed, Inc. · Aug 2011
REPROCESSED DIAGNOSTIC ULTRASOUND CATHETER
K033436 · Alliance Medical Corp. · Mar 2005
STERILEMED REPROCESSED IVUS IMAGING CATHETER
K043453 · Sterilmed, Inc. · Mar 2005
REPROCESSED IMAGING CATHETERS
K012537 · Sterilmed, Inc. · Oct 2002