LEOCOR CORFLO PUMP -- MODIFICATION— 510(k) K924110

Name: FDA 510(k) clearance K924110
Creator: U.S. Food and Drug Administration
Published: 1992-09-01

Substantially Equivalent

Leocor, Inc.

FDA 510(k) clearance K924110 for LEOCOR CORFLO PUMP -- MODIFICATION, Substantially Equivalent on 1992-09-01. Applicant: Leocor, Inc.. Device class: 2.

Clearance details

Applicant: Leocor, Inc.
Product code: Code DQI
Device class: Class 2
Regulation: 21 CFR 870.1800
Advisory panel: Cardiovascular
Date received: 1992-06-03
Decision date: 1992-09-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.