FDA 510(k)

MICRUS MICROCOIL SYSTEMS

K-Number: K073442 · 2008-02-26

ApplicantMicrus Endovascular Corporation

Decision Date2008-02-26

Product CodeHCG

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

MICRUS MICROCOIL SYSTEMS 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 2008-02-26 under 510(k) number K073442. The device is classified under product code HCG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRUS MICROCOIL SYSTEMS?

MICRUS MICROCOIL SYSTEMS is a medical device that received FDA 510(k) clearance on 2008-02-26. The listed applicant is Micrus Endovascular Corporation. The 510(k) number is K073442.

When did MICRUS MICROCOIL SYSTEMS receive FDA 510(k) clearance?

MICRUS MICROCOIL SYSTEMS received FDA 510(k) clearance on 2008-02-26, under 510(k) number K073442.

Who is the listed applicant for MICRUS MICROCOIL SYSTEMS?

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 MICROCOIL SYSTEMS?

The FDA product code for MICRUS MICROCOIL SYSTEMS is HCG.

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Other records listing Micrus Endovascular Corporation as applicant

K103780MICRUS ASCENT OCCLUSION BALLOON CATHETER 4X7 MM; MICRUS ASCENT OCCLUSION BALLOON CATHETER 6X9 MM; MICRUS SUMMIT OCCLUSIO K102818MICRUS ONE 2 ONE GUIDEWIRE, MICRUS ONE 2 ONE SOFT GUIDEWIRE K092702MICRUS MICROCATHETER, MODEL COURIER 270 K091504MICRUS ASCENT OCCLUSION BALLOON CATHETER 4X7MM,6X9MM, MICRUS SUMMIT OCCLUSION BALLOON CATHETER 4X10MM,4X15, MODEL BRS 00 K083922MICRUS MICROCATHETER, COURIER FLEX, MODEL MSF 170000-00 K090274MICRUS ONE 2 ONE GUIDEWIRE AND SOFT GUIDEWIRE

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Related Devices (Code: HCG)

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.