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FDA 510(k) Applications Submitted by FLEXMEDICS
FDA 510(k) Number
Submission Date
Device Name
Applicant
K964955
12/11/1996
FLEXFINDER GUIDEWIRE (REGULAR SHAFT/STIFF SHAFT) MARKED INK BANDS ENCAP+/GUIDEWIRE(REGULAR SHAFT/STIFF SHAFT) NO MARKING
FLEXMEDICS
K990765
03/08/1999
FLEXFINDER GUIDE WIRE(REGULAR SHAFT/STIFF SHAFT) MARKED INK BANDS, FLEXFINDER GUIDE WIRE (REGULAR SHAFT/STIFF SHAFT) NO
FLEXMEDICS
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