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FDA 510(k)

HI-TORQUE SPORT-T(TM) GUIDE WIRE

K-Number: K915554 · 1993-02-09

ApplicantPeripheral Systems Group
Decision Date1993-02-09
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HI-TORQUE SPORT-T(TM) GUIDE WIRE is the device name listed in this FDA 510(k) record. The listed applicant is Peripheral Systems Group. It received FDA 510(k) clearance on 1993-02-09 under 510(k) number K915554. 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 HI-TORQUE SPORT-T(TM) GUIDE WIRE?

HI-TORQUE SPORT-T(TM) GUIDE WIRE is a medical device that received FDA 510(k) clearance on 1993-02-09. The listed applicant is Peripheral Systems Group. The 510(k) number is K915554.

When did HI-TORQUE SPORT-T(TM) GUIDE WIRE receive FDA 510(k) clearance?

HI-TORQUE SPORT-T(TM) GUIDE WIRE received FDA 510(k) clearance on 1993-02-09, under 510(k) number K915554.

Who is the listed applicant for HI-TORQUE SPORT-T(TM) GUIDE WIRE?

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

What is the FDA product code for HI-TORQUE SPORT-T(TM) GUIDE WIRE?

The FDA product code for HI-TORQUE SPORT-T(TM) GUIDE WIRE is DQX.

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Other records listing Peripheral Systems Group 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.

K940804SMARTNEEDLE VASCULAR ACCESS SYSTEM, MODIFICATIONK934433VANTAGE DIALTAION CATHETERK932777SMARTNEEDLE(R) OVER-THE-NEEDLE CATHETERK931327PSG DIRECTIONAL HYDROPHILIC GUIDE WIREK914979EDM(R) INFUSION CATHETERK913941PSG(TM) 20 GUAGE DOPPLER NEEDLE

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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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