FDA 510(k) Applications Submitted by GYRUS MEDICAL LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K041285 05/13/2004 GYRUS G3 SYSTEM (GENERATOR, ASSESSORIES, SOMNOPLASTY ELECTRODES AND PLASMACISION ELECTRODES) GYRUS MEDICAL LTD.
K990628 02/25/1999 GYRUS ENDOUROLOGY SYSTEM GYRUS MEDICAL LTD.
K001270 04/20/2000 GYRUS ENDOUROLOGY SYSTEM: AXIPOLAR RESECTOSCOPE LOOP ELECTRODE GYRUS MEDICAL LTD.
K982771 08/07/1998 GYRUS HYSTEROSCOPIC RESECTOSCOPE GYRUS MEDICAL LTD.
K993749 11/05/1999 GYRUS HYSTEROSCOPIC RESECTOSCOPE GYRUS MEDICAL LTD.
K003569 11/20/2000 PLASMAKINETIC ENDOUROLOGY SYSTEM GYRUS MEDICAL LTD.
K994166 12/09/1999 GYRUS ENDOUROLOGY SYSTEM: AXIPOLAR RESECTOSCOPE ELECTRODE GYRUS MEDICAL LTD.


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