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FDA 510(k) Applications Submitted by JOHN CORZINE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K990379
02/08/1999
MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIES
DEXIDE, INC.
K991814
05/27/1999
MULTACHOICE INSTRUMENTS
DEXIDE, INC.
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