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FDA 510(k)

MICRUS ASCENT OCCLUSION BALLOON CATHETER

K-Number: K080861 · 2008-08-27

ApplicantMicrus Endovascular Corporation
Decision Date2008-08-27
Product CodeMJN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MICRUS ASCENT OCCLUSION BALLOON CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Micrus Endovascular Corporation. It received FDA 510(k) clearance on 2008-08-27 under 510(k) number K080861. The device is classified under product code MJN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRUS ASCENT OCCLUSION BALLOON CATHETER?

MICRUS ASCENT OCCLUSION BALLOON CATHETER is a medical device that received FDA 510(k) clearance on 2008-08-27. The listed applicant is Micrus Endovascular Corporation. The 510(k) number is K080861.

When did MICRUS ASCENT OCCLUSION BALLOON CATHETER receive FDA 510(k) clearance?

MICRUS ASCENT OCCLUSION BALLOON CATHETER received FDA 510(k) clearance on 2008-08-27, under 510(k) number K080861.

Who is the listed applicant for MICRUS ASCENT OCCLUSION BALLOON CATHETER?

The FDA 510(k) record lists Micrus Endovascular Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICRUS ASCENT OCCLUSION BALLOON CATHETER?

The FDA product code for MICRUS ASCENT OCCLUSION BALLOON CATHETER is MJN.

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Other records listing Micrus Endovascular Corporation as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K103780MICRUS ASCENT OCCLUSION BALLOON CATHETER 4X7 MM; MICRUS ASCENT OCCLUSION BALLOON CATHETER 6X9 MM; MICRUS SUMMIT OCCLUSIOK102818MICRUS ONE 2 ONE GUIDEWIRE, MICRUS ONE 2 ONE SOFT GUIDEWIREK092702MICRUS MICROCATHETER, MODEL COURIER 270K091504MICRUS ASCENT OCCLUSION BALLOON CATHETER 4X7MM,6X9MM, MICRUS SUMMIT OCCLUSION BALLOON CATHETER 4X10MM,4X15, MODEL BRS 00K083922MICRUS MICROCATHETER, COURIER FLEX, MODEL MSF 170000-00K090274MICRUS ONE 2 ONE GUIDEWIRE AND SOFT GUIDEWIRE

View all 23 devices →

Related Devices (Code: MJN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K243795pREBOA-PRO CatheterPrytime Medical Devices, Inc.K251358Bridge Plus Occlusion Balloon (590-002)Philips Image Guided Therapy DevicesK221294preCARDIA Occlusion SystemAbiomed, Inc.K214060LANDMARK REBOA CatheterZien Medical Technologies, Inc.K211610Fogarty Occlusion CatheterEdwards Lifesciences, LLCK212324RenovoCathRenovorx, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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