FDA 510(k)

CARDI0METRICS FLOW WIRE XT DOPPLER GUIDE MODEL 1403, 1404

K-Number: K955551 · 1996-02-28

Decision Date1996-02-28

Product CodeDQX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CARDI0METRICS FLOW WIRE XT DOPPLER GUIDE MODEL 1403, 1404 is the device name listed in this FDA 510(k) record. The listed applicant is Cardio Metrics, Inc.. It received FDA 510(k) clearance on 1996-02-28 under 510(k) number K955551. 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 CARDI0METRICS FLOW WIRE XT DOPPLER GUIDE MODEL 1403, 1404?

CARDI0METRICS FLOW WIRE XT DOPPLER GUIDE MODEL 1403, 1404 is a medical device that received FDA 510(k) clearance on 1996-02-28. The listed applicant is Cardio Metrics, Inc.. The 510(k) number is K955551.

When did CARDI0METRICS FLOW WIRE XT DOPPLER GUIDE MODEL 1403, 1404 receive FDA 510(k) clearance?

CARDI0METRICS FLOW WIRE XT DOPPLER GUIDE MODEL 1403, 1404 received FDA 510(k) clearance on 1996-02-28, under 510(k) number K955551.

Who is the listed applicant for CARDI0METRICS FLOW WIRE XT DOPPLER GUIDE MODEL 1403, 1404?

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

What is the FDA product code for CARDI0METRICS FLOW WIRE XT DOPPLER GUIDE MODEL 1403, 1404?

The FDA product code for CARDI0METRICS FLOW WIRE XT DOPPLER GUIDE MODEL 1403, 1404 is DQX.

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Other records listing Cardio Metrics, Inc. as applicant

K972762CARDIOMETRICS FLOWIRE 300 AND XT 300 DOPPLER GUIDE WIRES K965140CARDIOMETRICS WAVEWIRE/WAVEMAP PRESSURE SYSTEM K951567CARDIOMETICS FLOWIRE, SMARTWIRE DOPPLER GUIDE WIRE K961777ACCUTRAC XT INTRAVASCULAR GUIDE WIRE (FLOPPY) MODEL 2403/(FLEX) MODEL 2404 K954913CARDIOMETRICS ACCUTRAC INTRAVASCULAR GUIDE WIRE (MODIFICATION)K952562CARDIOMETRICS ACCUTRAC INTRAVASCULAR GUIDE WIRE

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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.