Cleared Traditional

K152194 - transGlide Expandable Introducer

K152194 is an FDA 510(k) clearance for transGlide Expandable Introducer, manufactured by Transaortic Medical, Inc.. The device is a Class 2 Cardiovascular device with product code DYB cleared through the Traditional 510(k) pathway after a 246-day FDA review.

K152194 · Transaortic Medical, Inc. · Cardiovascular device
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Apr 2016
Decision
246d
Days
Class 2
Risk

K152194 is an FDA 510(k) clearance for the transGlide Expandable Introducer. Classified as Introducer, Catheter (product code DYB), Class II - Special Controls.

Submitted by Transaortic Medical, Inc. (Morgan Hill, US). The FDA issued a Cleared decision on April 7, 2016 after a review of 246 days - an extended review 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: 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 Transaortic Medical, Inc. devices

FDA 510(k) Submission Details - K152194

510(k) Number K152194 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 05, 2015
Decision Date April 07, 2016
Days to Decision 246 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
121d slower than avg
Panel avg: 125d · This submission: 246d
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 598
Devices cleared under the same product code (DYB) and FDA review panel - the closest regulatory comparables to K152194.
Nanostim Introducer Kit
K161102 · St. Jude Medical, Inc. · May 2016
GORE DrySeal Flex Introducer Sheath
K160254 · W.L. Gore & Associates, Inc. · May 2016
The Nanostim Introducer Kit
K160716 · St. Jude Medical, Inc. · Apr 2016
Flexor Tuohy-Borst Side-Arm Introducers Shuttle Select
K153430 · Cook Incorporated · Mar 2016
Endophys Pressure Sensing Sheath Kit
K160272 · Endophys, Inc. · Mar 2016
PTFE Super Sheath Introducer 2.1
K153246 · Medcomp (Medical Components, Inc.) · Feb 2016