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FDA 510(k)

SCHNEIDER SOLID-7 SOPTIP GUIDING CATHETER

K-Number: K924591 · 1992-12-08

ApplicantSchneider Intl., Ltd.
Decision Date1992-12-08
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SCHNEIDER SOLID-7 SOPTIP GUIDING CATHETER 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 1992-12-08 under 510(k) number K924591. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCHNEIDER SOLID-7 SOPTIP GUIDING CATHETER?

SCHNEIDER SOLID-7 SOPTIP GUIDING CATHETER is a medical device that received FDA 510(k) clearance on 1992-12-08. The listed applicant is Schneider Intl., Ltd.. The 510(k) number is K924591.

When did SCHNEIDER SOLID-7 SOPTIP GUIDING CATHETER receive FDA 510(k) clearance?

SCHNEIDER SOLID-7 SOPTIP GUIDING CATHETER received FDA 510(k) clearance on 1992-12-08, under 510(k) number K924591.

Who is the listed applicant for SCHNEIDER SOLID-7 SOPTIP GUIDING CATHETER?

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 SOLID-7 SOPTIP GUIDING CATHETER?

The FDA product code for SCHNEIDER SOLID-7 SOPTIP GUIDING CATHETER is DQY.

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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 SYSTEMK931577SCHNEIDER MAGNUM PERIPHERAL RECANALIZATION GUIDEWIK926003SCHNEIDER SOFTIP SST ANGIOGRAPHIC (DIAG) CATHETERK926271SCHNEIDER MATCH-35 PERCUTANEOUS TRANSLUMINAL ANGIOK925804SCHNEIDER HYDRO-SIL GUIDEWIREK921856TOTAL CROSS .021 PERCUT. TRANSLUMINAL ANGIO. CATH.

View all 22 devices →

Related Devices (Code: DQY)

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.

K262817CrossFAST Integrated Microcatheter Advanced Delivery SystemVantis Vascular, Inc.K260559NHanceITIMDS Operation B.V.K262392APRO 35 Swift CatheterAlembic, LLCK262240SSPC NXT Delivery CatheterCenterPoint Systems, LLCK261766CPS Locator 3D Plus Delivery CatheterCenterPoint Systems, LLCK261825Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP CatheterAbbott

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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