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FDA 510(k)

LEOCOR GUIDING CATHETER

K-Number: K911270 · 1992-01-17

ApplicantLeocor, Inc.
Decision Date1992-01-17
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LEOCOR GUIDING CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Leocor, Inc.. It received FDA 510(k) clearance on 1992-01-17 under 510(k) number K911270. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEOCOR GUIDING CATHETER?

LEOCOR GUIDING CATHETER is a medical device that received FDA 510(k) clearance on 1992-01-17. The listed applicant is Leocor, Inc.. The 510(k) number is K911270.

When did LEOCOR GUIDING CATHETER receive FDA 510(k) clearance?

LEOCOR GUIDING CATHETER received FDA 510(k) clearance on 1992-01-17, under 510(k) number K911270.

Who is the listed applicant for LEOCOR GUIDING CATHETER?

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

What is the FDA product code for LEOCOR GUIDING CATHETER?

The FDA product code for LEOCOR GUIDING CATHETER is DQO.

Related Clinical Trials

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.

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Other records listing Leocor, Inc. 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.

K924110LEOCOR CORFLO PUMP -- MODIFICATIONK900350LEOCOR CORFLO(TM) PUMP

Related Devices (Code: DQO)

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.

K261455Arterial Pressure Monitoring Set/TraySpectrum VascularK252702Bioptimal Pulmonary Artery Monitoring Catheter (TD2502NF, TD2502NGF, TD2502NDF, TD2502NCF, TD2502NCGF, TD2502NDGF, TD2502NDCF, TD2502NDCGF, TD2502NXCF, TD2502NDXF, TD2502NXCGF, TD2502NDXGF, TD2502NDXCF, TD2502NDXCGF, TD2502-110NF, TD2502-110NGF, TD2502-110NDF, TD2502-110NCF, TD2502-110NDGF, TD2502-110NDCF, TD2502-110NCGF, TD2502-110NDCGF, TD2502-110NXF, TD2502-110NXGF, TD2502-110NDXF, TD2502-110NXCF, TD2502-110NDXGF, TD2502-110NDXCF ,TD2502-110NXCGF, TD2502-110NDXCGF, TD2602NF, TD2602NBioptimal International Pte. , Ltd.K254278Arterial Pressure Monitoring Set/TraySpectrum VascularK250751DualView CatheterTerumo CorporationK242966Gentuity® HF-OCT Imaging System with Vis-Rx Prime® Micro-Imaging CatheterGentuity, LLCK242420pNOVUS 21 MicrocatheterPhenox, Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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