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FDA 510(k)

SCHNEIDER MAGNUM PERIPHERAL RECANALIZATION GUIDEWI

K-Number: K931577 · 1993-06-23

ApplicantSchneider Intl., Ltd.
Decision Date1993-06-23
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SCHNEIDER MAGNUM PERIPHERAL RECANALIZATION GUIDEWI is the device name listed in this FDA 510(k) record. The listed applicant is Schneider Intl., Ltd.. It received FDA 510(k) clearance on 1993-06-23 under 510(k) number K931577. 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 SCHNEIDER MAGNUM PERIPHERAL RECANALIZATION GUIDEWI?

SCHNEIDER MAGNUM PERIPHERAL RECANALIZATION GUIDEWI is a medical device that received FDA 510(k) clearance on 1993-06-23. The listed applicant is Schneider Intl., Ltd.. The 510(k) number is K931577.

When did SCHNEIDER MAGNUM PERIPHERAL RECANALIZATION GUIDEWI receive FDA 510(k) clearance?

SCHNEIDER MAGNUM PERIPHERAL RECANALIZATION GUIDEWI received FDA 510(k) clearance on 1993-06-23, under 510(k) number K931577.

Who is the listed applicant for SCHNEIDER MAGNUM PERIPHERAL RECANALIZATION GUIDEWI?

The FDA 510(k) record lists Schneider Intl., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SCHNEIDER MAGNUM PERIPHERAL RECANALIZATION GUIDEWI?

The FDA product code for SCHNEIDER MAGNUM PERIPHERAL RECANALIZATION GUIDEWI is DQX.

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Other records listing Schneider Intl., Ltd. 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.

K925406BILIARY ENDOPROSTHESES W/UNISTEP DELIVERY SYSTEMK926271SCHNEIDER MATCH-35 PERCUTANEOUS TRANSLUMINAL ANGIOK926003SCHNEIDER SOFTIP SST ANGIOGRAPHIC (DIAG) CATHETERK925804SCHNEIDER HYDRO-SIL GUIDEWIREK924591SCHNEIDER SOLID-7 SOPTIP GUIDING CATHETERK921856TOTAL CROSS .021 PERCUT. TRANSLUMINAL ANGIO. CATH.

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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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