Gyrus Medical , Ltd.
Gyrus Medical , Ltd. holds FDA 510(k) medical device clearances, first cleared 1990, most recent 2004.
Top product codes for Gyrus Medical , Ltd.
Recent clearances by Gyrus Medical , Ltd.
- K041285 — GYRUS G3 SYSTEM (GENERATOR, ASSESSORIES, SOMNOPLASTY ELECTRODES AND PLASMACISION ELECTRODES)
- K003569 — PLASMAKINETIC ENDOUROLOGY SYSTEM
- K001270 — GYRUS ENDOUROLOGY SYSTEM: AXIPOLAR RESECTOSCOPE LOOP ELECTRODE
- K994166 — GYRUS ENDOUROLOGY SYSTEM: AXIPOLAR RESECTOSCOPE ELECTRODE
- K993749 — GYRUS HYSTEROSCOPIC RESECTOSCOPE
- K990628 — GYRUS ENDOUROLOGY SYSTEM
- K982771 — GYRUS HYSTEROSCOPIC RESECTOSCOPE
- K891681 — DILECTRON URINARY CONDUCTIVITY PROBE
Data sourced from openFDA. This site is unofficial and independent of the FDA.