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FDA 510(k)

FINISHING WIRE SUPPORTRAK

K-Number: K041762 · 2004-08-06

ApplicantGuidant Corporation
Decision Date2004-08-06
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

FINISHING WIRE SUPPORTRAK is the device name listed in this FDA 510(k) record. The listed applicant is Guidant Corporation. It received FDA 510(k) clearance on 2004-08-06 under 510(k) number K041762. 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 FINISHING WIRE SUPPORTRAK?

FINISHING WIRE SUPPORTRAK is a medical device that received FDA 510(k) clearance on 2004-08-06. The listed applicant is Guidant Corporation. The 510(k) number is K041762.

When did FINISHING WIRE SUPPORTRAK receive FDA 510(k) clearance?

FINISHING WIRE SUPPORTRAK received FDA 510(k) clearance on 2004-08-06, under 510(k) number K041762.

Who is the listed applicant for FINISHING WIRE SUPPORTRAK?

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

What is the FDA product code for FINISHING WIRE SUPPORTRAK?

The FDA product code for FINISHING WIRE SUPPORTRAK is DQX.

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Other records listing Guidant Corporation 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.

K060449HI-TORQUE ADVANCE AND ADVANCE LITE GUIDE WIREK053459OMNILINK .035 BILIARY STENT SYSTEMK053454RX HERCULINK ELITE BILIARY STENT SYSTEMK053019ACUITY STEERABLE STYLET ACCESSORYK052965EASYTRAK 2 STYLET, MODELS 4826, 4829, 4832.K052274GUIDANT VASOVIEW HEMOPRO ENDOSCOPIC VESSEL HARVESTING SYSTEM, MODEL VH-3000

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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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