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FDA 510(k)

NEUROVASX SUB-MICROINFUSION CATHETER

K-Number: K984258 · 1999-02-11

ApplicantNeuro Vasx, Inc.
Decision Date1999-02-11
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NEUROVASX SUB-MICROINFUSION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Neuro Vasx, Inc.. It received FDA 510(k) clearance on 1999-02-11 under 510(k) number K984258. 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 NEUROVASX SUB-MICROINFUSION CATHETER?

NEUROVASX SUB-MICROINFUSION CATHETER is a medical device that received FDA 510(k) clearance on 1999-02-11. The listed applicant is Neuro Vasx, Inc.. The 510(k) number is K984258.

When did NEUROVASX SUB-MICROINFUSION CATHETER receive FDA 510(k) clearance?

NEUROVASX SUB-MICROINFUSION CATHETER received FDA 510(k) clearance on 1999-02-11, under 510(k) number K984258.

Who is the listed applicant for NEUROVASX SUB-MICROINFUSION CATHETER?

The FDA 510(k) record lists Neuro Vasx, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEUROVASX SUB-MICROINFUSION CATHETER?

The FDA product code for NEUROVASX SUB-MICROINFUSION CATHETER 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 Neuro Vasx, Inc. 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.

K011646NEUROEDGE INFUSION CATHETER

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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