FDA 510(k)

ACS HI-TORQUE WHOLEY SUPRA CORE GUIDE WIRE

K-Number: K980119 · 1998-03-20

Decision Date1998-03-20

Product CodeDQX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

ACS HI-TORQUE WHOLEY SUPRA CORE GUIDE WIRE is the device name listed in this FDA 510(k) record. The listed applicant is Guidant Corp.. It received FDA 510(k) clearance on 1998-03-20 under 510(k) number K980119. 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 ACS HI-TORQUE WHOLEY SUPRA CORE GUIDE WIRE?

ACS HI-TORQUE WHOLEY SUPRA CORE GUIDE WIRE is a medical device that received FDA 510(k) clearance on 1998-03-20. The listed applicant is Guidant Corp.. The 510(k) number is K980119.

When did ACS HI-TORQUE WHOLEY SUPRA CORE GUIDE WIRE receive FDA 510(k) clearance?

ACS HI-TORQUE WHOLEY SUPRA CORE GUIDE WIRE received FDA 510(k) clearance on 1998-03-20, under 510(k) number K980119.

Who is the listed applicant for ACS HI-TORQUE WHOLEY SUPRA CORE GUIDE WIRE?

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

What is the FDA product code for ACS HI-TORQUE WHOLEY SUPRA CORE GUIDE WIRE?

The FDA product code for ACS HI-TORQUE WHOLEY SUPRA CORE GUIDE WIRE is DQX.

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Other records listing Guidant Corp. as applicant

K061865FLEX 10 MIS ABLATION PROBE, MODEL FLX10MI-05 K061453HI-TORQUE WHISPER VIEW GUIDE WIRE K042908RX ACCUNET 2 EMBOLIC PROTECTION SYSTEM K042218ACCUNET EMBOLIC PROTECTION SYSTEM, RX ACCUNET EMBOLIC PROTECTION SYSTEM K033834OMNILINK .018 BILIARY STENT SYSTEM K033393ABSOLUTE .035 SELF-EXPANDING BILIARY STENT SYSTEM

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Related Devices (Code: DQX)

K253146Hyperdrive 35 GuidewireRapid-Medical , Ltd.K261281CROSSLEAD Standard 035 and CROSSLEAD Stiff 035Filmecc Co., Ltd.K253667Accoat Guide WireSp Medical A/S K261640Merit 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.