Cleared Traditional

K141696 - EDWARDS ESHEATH INTRODUCER SET

K141696 is an FDA 510(k) clearance for EDWARDS ESHEATH INTRODUCER SET, manufactured by Edwards Lifesciences. The device is a Class 2 Cardiovascular device with product code DYB cleared through the Traditional 510(k) pathway after a 86-day FDA review.

K141696 · Edwards Lifesciences · Cardiovascular device
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Sep 2014
Decision
86d
Days
Class 2
Risk

K141696 is an FDA 510(k) clearance for the EDWARDS ESHEATH INTRODUCER SET. Classified as Introducer, Catheter (product code DYB), Class II - Special Controls.

Submitted by Edwards Lifesciences (Irvine, US). The FDA issued a Cleared decision on September 18, 2014 after a review of 86 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 Edwards Lifesciences devices

FDA 510(k) Submission Details - K141696

510(k) Number K141696 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 24, 2014
Decision Date September 18, 2014
Days to Decision 86 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
39d faster than avg
Panel avg: 125d · This submission: 86d
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 433
Devices cleared under the same product code (DYB) and FDA review panel - the closest regulatory comparables to K141696.
NANOSTIM INTRODUCER KIT
K140793 · St. Jude Medical, Inc. · Dec 2014
PRELUDEEASE HYDROPHILIC SHEATH INTRODUCER
K140543 · Merit Medical Systems, Inc. · Oct 2014
FLEXOR RADIAL HYDROPHILIC INTRODUCER ACCESS SET
K132592 · Cook, Inc. · Oct 2014
MERIT SAFETY INTRODUCER NEEDLE
K140513 · Merit Medical Systems, Inc. · Jul 2014
INTRODUCER, MODEL ADELANTE MAGNUM
K140917 · Oscor, Inc. · Jul 2014
MICROPUNCTURE INTRODUCER SET
K133114 · Cook Incorporated · Jul 2014