Cleared Traditional

K142692 - Occlusion Balloon Catheter

K142692 is an FDA 510(k) clearance for Occlusion Balloon Catheter, manufactured by Embolx, Inc.. The device is a Class 2 Cardiovascular device with product code MJN cleared through the Traditional 510(k) pathway after a 251-day FDA review.

K142692 · Embolx, Inc. · Cardiovascular device
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May 2015
Decision
251d
Days
Class 2
Risk

K142692 is an FDA 510(k) clearance for the Occlusion Balloon Catheter. Classified as Catheter, Intravascular Occluding, Temporary (product code MJN), Class II - Special Controls.

Submitted by Embolx, Inc. (Los Altos, US). The FDA issued a Cleared decision on May 31, 2015 after a review of 251 days - an extended review cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.4450 - 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 Embolx, Inc. devices

FDA 510(k) Submission Details - K142692

510(k) Number K142692 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 22, 2014
Decision Date May 31, 2015
Days to Decision 251 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
126d slower than avg
Panel avg: 125d · This submission: 251d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MJN Device Classification - Class 2, Special Controls

Product Code MJN Catheter, Intravascular Occluding, Temporary
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.4450
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 - MJN Catheter, Intravascular Occluding, Temporary

All 60
Devices cleared under the same product code (MJN) and FDA review panel - the closest regulatory comparables to K142692.
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EQUALIZER OCCLUSION BALLOON CATHETER
K140273 · Boston Scientific Corp · Jul 2014
LEMAITRE 8F OCCLUSION CATHETER
K132022 · LeMaitre Vascular, Inc. · Nov 2013
OCCLUSION BALLOON CATHETER
K132990 · Boston Scientific Corp · Oct 2013