Medionics International , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medionics International , Ltd. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Medionics International , Ltd. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1982 to 1992. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Medionics International , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medionics International , Ltd.
6 devices
Cleared
Jan 13, 1992
SELECTRA AND TUBING SETS
Gastroenterology & Urology
363d
Cleared
Nov 03, 1988
CAPD DISPOSABLE Y SYSTEM - DY SET
Gastroenterology & Urology
86d
Cleared
Jun 25, 1984
C.A.P.D. AUTOMATIC HEATER PDH 200
Gastroenterology & Urology
13d
Cleared
Oct 14, 1983
MICROSTAR VCI
Gastroenterology & Urology
135d
Cleared
Oct 14, 1983
MICROSTAR VC1 VOLUMETRIC CYCLER
Gastroenterology & Urology
101d
Cleared
Jul 28, 1982
C.A.P.D. AUTOMATIC HEATER #PDC 2000 HCP
Gastroenterology & Urology
85d