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

Substantially Equivalent

Leocor, Inc.

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

Clearance details

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

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