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FDA 510(k) Applications Submitted by TODD CASSIDY
FDA 510(k) Number
Submission Date
Device Name
Applicant
K010399
02/09/2001
DIATEK CANNON-CATH #CC2400, CC2800, CC3200, CC3600,CC5500. CC2400PC, CC2800PC, CC3200PC(32 CM), CC3200PC(36 CM)
DIATEK, INC.
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