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FDA 510(k) Applications Submitted by MEDI-DYNE, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K970401
02/03/1997
MEDI-DYNE GUIDING CATHETER
MEDI-DYNE, INC.
K000825
03/14/2000
4F-7F MEDI-DYNE TORQ FLOW XLB ANGIOGRAPHIC CATHETER
MEDI-DYNE, INC.
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