Cleared Traditional

K030723 - IVS INTRODUCER SET, MODEL 1003

K030723 is an FDA 510(k) clearance for IVS INTRODUCER SET, manufactured by Integrated Vascular Systems, Inc.. The device is a Class 2 Cardiovascular device with product code DYB cleared through the Traditional 510(k) pathway after a 27-day FDA review.

K030723 · Integrated Vascular Systems, Inc. · Cardiovascular device
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Apr 2003
Decision
27d
Days
Class 2
Risk

K030723 is an FDA 510(k) clearance for the IVS INTRODUCER SET, MODEL 1003. Classified as Introducer, Catheter (product code DYB), Class II - Special Controls.

Submitted by Integrated Vascular Systems, Inc. (Sunnyvale, US). The FDA issued a Cleared decision on April 3, 2003 after a review of 27 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1340 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Integrated Vascular Systems, Inc. devices

FDA 510(k) Submission Details - K030723

510(k) Number K030723 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 07, 2003
Decision Date April 03, 2003
Days to Decision 27 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
98d faster than avg
Panel avg: 125d · This submission: 27d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DYB Device Classification - Class 2, Special Controls

Product Code DYB Introducer, Catheter
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1340
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 - DYB Introducer, Catheter

All 568
Devices cleared under the same product code (DYB) and FDA review panel - the closest regulatory comparables to K030723.
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K023447 · St Jude Medical · Oct 2002
MEDCOMP VASCU-SHEATH INTRODUCER SET
K022513 · Medcomp · Oct 2002