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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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