Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

JS VASCULAR GUIDE WIRE VISE/TORQUE DEVICE

K-Number: K032411 · 2003-10-07

ApplicantJs Vascular, Inc.
Decision Date2003-10-07
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

JS VASCULAR GUIDE WIRE VISE/TORQUE DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Js Vascular, Inc.. It received FDA 510(k) clearance on 2003-10-07 under 510(k) number K032411. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JS VASCULAR GUIDE WIRE VISE/TORQUE DEVICE?

JS VASCULAR GUIDE WIRE VISE/TORQUE DEVICE is a medical device that received FDA 510(k) clearance on 2003-10-07. The listed applicant is Js Vascular, Inc.. The 510(k) number is K032411.

When did JS VASCULAR GUIDE WIRE VISE/TORQUE DEVICE receive FDA 510(k) clearance?

JS VASCULAR GUIDE WIRE VISE/TORQUE DEVICE received FDA 510(k) clearance on 2003-10-07, under 510(k) number K032411.

Who is the listed applicant for JS VASCULAR GUIDE WIRE VISE/TORQUE DEVICE?

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

What is the FDA product code for JS VASCULAR GUIDE WIRE VISE/TORQUE DEVICE?

The FDA product code for JS VASCULAR GUIDE WIRE VISE/TORQUE DEVICE is DQX.

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

Related Devices (Code: DQX)

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.

K253146Hyperdrive 35 GuidewireRapid-Medical , Ltd.K261281CROSSLEAD Standard 035 and CROSSLEAD Stiff 035Filmecc Co., Ltd.K253667Accoat Guide WireSp Medical A/SK261640Merit MAK Nitinol/Gold-Tungsten Guide WireMerit Medical Ireland , Ltd.K254137InQwire Amplatz Guide WireMerit Medical Ireland, Ltd.K260544FMD Peripheral Guide Wire F-14 Flex 6; FMD Peripheral Guide Wire F-14 Tapered 40; FMD Peripheral Guide Wire F-18 Flex SP; FMD Peripheral Guide Wire F-18 DP 25; FMD Peripheral Guide Wire F-18 Tapered 40FMD Co., Ltd.

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.

↑