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FDA 510(k)

LEOCOR CORFLO PUMP -- MODIFICATION

K-Number: K924110 · 1992-09-01

ApplicantLeocor, Inc.
Decision Date1992-09-01
Product CodeDQI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LEOCOR CORFLO PUMP -- MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Leocor, Inc.. It received FDA 510(k) clearance on 1992-09-01 under 510(k) number K924110. The device is classified under product code DQI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEOCOR CORFLO PUMP -- MODIFICATION?

LEOCOR CORFLO PUMP -- MODIFICATION is a medical device that received FDA 510(k) clearance on 1992-09-01. The listed applicant is Leocor, Inc.. The 510(k) number is K924110.

When did LEOCOR CORFLO PUMP -- MODIFICATION receive FDA 510(k) clearance?

LEOCOR CORFLO PUMP -- MODIFICATION received FDA 510(k) clearance on 1992-09-01, under 510(k) number K924110.

Who is the listed applicant for LEOCOR CORFLO PUMP -- MODIFICATION?

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 CORFLO PUMP -- MODIFICATION?

The FDA product code for LEOCOR CORFLO PUMP -- MODIFICATION is DQI.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K911270LEOCOR GUIDING CATHETERK900350LEOCOR CORFLO(TM) PUMP

Related Devices (Code: DQI)

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.

K960486KSEA MODEL 383320 20 ANGIOMATKarl Storz EndoscopyK935763SURGIPUMPW.O.M. World of Medicine GmbHK922541USCI SUPER 9 PTCA GUIDING CATHETERC.R. Bard, Inc.K905189BAXTER ANGIOSCOPY PUMP TUBING SET (MODEL NL)Baxter Healthcare CorpK902444CLEARVIEW(TM) ANGIOSCOPIC IRRIGATION PUMPIntramed Laboratories, Inc.K895688NOBLES-LAI ENGINEERING INFUSION PUMPNobles-Lai Engineering, Inc.

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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