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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