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FDA 510(k)

STEREOTAXIS ENDOVASCULAR GUIDE WIRE

K-Number: K042854 · 2005-02-08

ApplicantStereotaxis, Inc.
Decision Date2005-02-08
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STEREOTAXIS ENDOVASCULAR GUIDE WIRE is the device name listed in this FDA 510(k) record. The listed applicant is Stereotaxis, Inc.. It received FDA 510(k) clearance on 2005-02-08 under 510(k) number K042854. 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 STEREOTAXIS ENDOVASCULAR GUIDE WIRE?

STEREOTAXIS ENDOVASCULAR GUIDE WIRE is a medical device that received FDA 510(k) clearance on 2005-02-08. The listed applicant is Stereotaxis, Inc.. The 510(k) number is K042854.

When did STEREOTAXIS ENDOVASCULAR GUIDE WIRE receive FDA 510(k) clearance?

STEREOTAXIS ENDOVASCULAR GUIDE WIRE received FDA 510(k) clearance on 2005-02-08, under 510(k) number K042854.

Who is the listed applicant for STEREOTAXIS ENDOVASCULAR GUIDE WIRE?

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

What is the FDA product code for STEREOTAXIS ENDOVASCULAR GUIDE WIRE?

The FDA product code for STEREOTAXIS ENDOVASCULAR GUIDE WIRE is DQX.

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Other records listing Stereotaxis, Inc. as applicant

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K262744GenesisX RMNK253473SynchronyK251792Stereotaxis GenesisX RMN with Navigant ™ Workstation (NWS)K250590MAGiC Sweep™ EP Mapping CatheterK193147Stereotaxis Genesis RMN with Navigant Workstation (NWS) and Cardiodrive SystemK192775Niobe® Magnetic Navigation System (MNS) with Navigant Workstation (NWS) and Cardiodri

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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.

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