LEOCOR CORFLO(TM) PUMP— 510(k) K900350

Substantially Equivalent

Leocor, Inc.

FDA 510(k) clearance K900350 for LEOCOR CORFLO(TM) PUMP, Substantially Equivalent on 1990-07-17. Applicant: Leocor, Inc..

Clearance details

Applicant: Leocor, Inc.
Product code: Code DXK
Advisory panel: Cardiovascular
Date received: 1990-01-24
Decision date: 1990-07-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Webster, TX, US

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