FDA 510(k)

BUCHBINDER MULTIFLEX GUIDEWIRE

K-Number: K884274 · 1988-12-27

Decision Date1988-12-27

Product CodeDQX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

BUCHBINDER MULTIFLEX GUIDEWIRE is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1988-12-27 under 510(k) number K884274. 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 BUCHBINDER MULTIFLEX GUIDEWIRE?

BUCHBINDER MULTIFLEX GUIDEWIRE is a medical device that received FDA 510(k) clearance on 1988-12-27. The listed applicant is Medtronic Vascular. The 510(k) number is K884274.

When did BUCHBINDER MULTIFLEX GUIDEWIRE receive FDA 510(k) clearance?

BUCHBINDER MULTIFLEX GUIDEWIRE received FDA 510(k) clearance on 1988-12-27, under 510(k) number K884274.

Who is the listed applicant for BUCHBINDER MULTIFLEX GUIDEWIRE?

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

What is the FDA product code for BUCHBINDER MULTIFLEX GUIDEWIRE?

The FDA product code for BUCHBINDER MULTIFLEX GUIDEWIRE is DQX.

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Other records listing Medtronic Vascular as applicant

K232570Steerant™ Super Stiff Guidewire K2321906F Sherpa NX Balanced Guide Catheter, 7F Sherpa NX Balanced Guide Catheter K2301565F Launcher Guide Catheter, 6F Launcher Guide Catheter, 7F Launcher Guide Catheter, 8F Launcher Guide Catheter K220773Everest 20 Inflation Device and 3-way Stopcock (AC2200);Everest 30 Inflation Device and 3-way Stopcock (AC3200);Everest 20 Survival Kit containing:1. Everest 20 Device with 3-way Stopcock, 2. Piton Y-Adaptor ,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC2205P); Everest 30 Survival Kit containing:1. Everest 30 Device with 3-way Stopcock, 2. Piton Y-Adaptor,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC3205P)K192296Medtronic 6F Taiga Guiding Catheter K173515Admiral Xtreme

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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.