Occlusion Balloon Catheter

FDA 510(k) K142692 · Embolx, Inc.

Substantially Equivalent

510(k) numberK142692

Submission

Device name
Occlusion Balloon Catheter
Applicant
Embolx, Inc.
Los Altos, CA, US
Received
September 22, 2014
Decision date
May 31, 2015
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MJN – Catheter, Intravascular Occluding, Temporary
Device class
Class II (moderate risk)
Regulation
21 CFR 870.4450
Specialty
Cardiovascular

Other 510(k)s with product code MJN

510(k)DeviceApplicantDecision
K243795pREBOA-PRO CatheterMJN · Traditional Prytime Medical Devices, Inc.09/05/2025SE
K251358Bridge Plus Occlusion Balloon (590-002)MJN · Traditional Philips Image Guided Therapy Devices06/24/2025SE
K221294preCARDIA Occlusion SystemMJN · Traditional Abiomed, Inc.06/30/2023SESU
K214060LANDMARK REBOA CatheterMJN · Traditional Zien Medical Technologies, Inc.09/19/2022SE
K211610Fogarty Occlusion CatheterMJN · Traditional Edwards Lifesciences, LLC02/14/2022SE
K212324RenovoCathMJN · Special Renovorx, Inc.08/23/2021SE
K210602AortaSTAT Occlusion DeviceMJN · Traditional Renalpro Medical, Inc.07/09/2021SE
K210358Neurescue deviceMJN · Traditional Neurescue Aps05/21/2021SE
K201652COBRA-OS KitMJN · Traditional Front Line Medical Technologies, Inc.02/22/2021SESK
K203540Bridge Occlusion BalloonMJN · Special Spectranetics, Inc.12/23/2020SE

More from Spectranetics, Inc.

510(k)DeviceDecision
K232536Soldier MicrocatheterDQO · Traditional 02/23/2024SE
K180904Sniper Infusion Catheter with Balloon OcclusionMJN · Traditional 06/08/2018SE

Questions and answers

When was Occlusion Balloon Catheter cleared by the FDA?

Occlusion Balloon Catheter (K142692) received a 510(k) decision of Substantially Equivalent on May 31, 2015, 251 days after the submission was received.

What is the product code of K142692?

The FDA product code is MJN – Catheter, Intravascular Occluding, Temporary, a Class II (moderate risk) device regulated under 21 CFR 870.4450.