Gyrus Medical , Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Gyrus Medical , Ltd. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Gyrus Medical , Ltd. has 8 FDA 510(k) cleared medical devices. Based in England, GB.
Historical record: 8 cleared submissions from 1990 to 2004. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Gyrus Medical , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Gyrus Medical , Ltd.
8 devices
Cleared
Sep 10, 2004
GYRUS G3 SYSTEM (GENERATOR, ASSESSORIES, SOMNOPLASTY ELECTRODES AND...
General & Plastic Surgery
120d
Cleared
Dec 19, 2000
PLASMAKINETIC ENDOUROLOGY SYSTEM
Gastroenterology & Urology
29d
Cleared
Apr 28, 2000
GYRUS ENDOUROLOGY SYSTEM: AXIPOLAR RESECTOSCOPE LOOP ELECTRODE
Gastroenterology & Urology
8d
Cleared
Dec 27, 1999
GYRUS ENDOUROLOGY SYSTEM: AXIPOLAR RESECTOSCOPE ELECTRODE
Gastroenterology & Urology
18d
Cleared
Dec 03, 1999
GYRUS HYSTEROSCOPIC RESECTOSCOPE
Obstetrics & Gynecology
28d
Cleared
Jun 29, 1999
GYRUS ENDOUROLOGY SYSTEM
Gastroenterology & Urology
124d
Cleared
Jan 21, 1999
GYRUS HYSTEROSCOPIC RESECTOSCOPE
Obstetrics & Gynecology
167d
Cleared
May 01, 1990
DILECTRON URINARY CONDUCTIVITY PROBE
Chemistry
405d