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FDA 510(k)

MICRUS MICROCATHETER

K-Number: K032624 · 2003-09-10

ApplicantMicrus Corp.
Decision Date2003-09-10
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MICRUS MICROCATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Micrus Corp.. It received FDA 510(k) clearance on 2003-09-10 under 510(k) number K032624. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRUS MICROCATHETER?

MICRUS MICROCATHETER is a medical device that received FDA 510(k) clearance on 2003-09-10. The listed applicant is Micrus Corp.. The 510(k) number is K032624.

When did MICRUS MICROCATHETER receive FDA 510(k) clearance?

MICRUS MICROCATHETER received FDA 510(k) clearance on 2003-09-10, under 510(k) number K032624.

Who is the listed applicant for MICRUS MICROCATHETER?

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

What is the FDA product code for MICRUS MICROCATHETER?

The FDA product code for MICRUS MICROCATHETER is DQO.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Micrus Corp. 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.

K033813MICRUS MODIFIED MICROCOIL SYSTEM, CERECYTEK032872MICRUS MICROCOIL SYSTEMK031578MICRUS MICROCOIL SYSTEMS, MODELS HEL, SPH, STR, FSR AND HSRK022420MICRUS STRETCH-RESISTANT MICROCOIL SYSTEM, MSR01K002056MICRUS MICROCOIL DELIVERY SYSTEM, MDS03

Related Devices (Code: DQO)

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.

K261455Arterial Pressure Monitoring Set/TraySpectrum VascularK252702Bioptimal Pulmonary Artery Monitoring Catheter (TD2502NF, TD2502NGF, TD2502NDF, TD2502NCF, TD2502NCGF, TD2502NDGF, TD2502NDCF, TD2502NDCGF, TD2502NXCF, TD2502NDXF, TD2502NXCGF, TD2502NDXGF, TD2502NDXCF, TD2502NDXCGF, TD2502-110NF, TD2502-110NGF, TD2502-110NDF, TD2502-110NCF, TD2502-110NDGF, TD2502-110NDCF, TD2502-110NCGF, TD2502-110NDCGF, TD2502-110NXF, TD2502-110NXGF, TD2502-110NDXF, TD2502-110NXCF, TD2502-110NDXGF, TD2502-110NDXCF ,TD2502-110NXCGF, TD2502-110NDXCGF, TD2602NF, TD2602NBioptimal International Pte. , Ltd.K254278Arterial Pressure Monitoring Set/TraySpectrum VascularK250751DualView CatheterTerumo CorporationK242966Gentuity® HF-OCT Imaging System with Vis-Rx Prime® Micro-Imaging CatheterGentuity, LLCK242420pNOVUS 21 MicrocatheterPhenox, Ltd.

Official Source

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

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