Medigroup is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medigroup - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Medigroup has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 9 cleared submissions from 1983 to 1983. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Medigroup Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medigroup
9 devices
Cleared
May 09, 1983
MEDIGROUP LS-110 LIGHT SOURCE
Obstetrics & Gynecology
185d
Cleared
May 06, 1983
MEDIGROUP 2.2MM NEEDLESCOPE CANNULA&
Obstetrics & Gynecology
182d
Cleared
May 06, 1983
ST-610 NEEDLESCOPE STERILIZATION TRAY
Obstetrics & Gynecology
182d
Cleared
May 05, 1983
MEDIGROUP LG-102 LIGHT GUIDE
Obstetrics & Gynecology
181d
Cleared
Jan 26, 1983
PC-205 TENCKHOFF CATHETER ROD OBTURATOR
Gastroenterology & Urology
82d
Cleared
Jan 26, 1983
QUILL CATHETER GUIDE
Gastroenterology & Urology
82d
Cleared
Jan 26, 1983
DIALATORS PC-203 & 202
Gastroenterology & Urology
79d
Cleared
Jan 26, 1983
PC-204 TUNNELOR
Gastroenterology & Urology
79d
Cleared
Jan 26, 1983
PC 201A LOCKING SLEEVE
Gastroenterology & Urology
82d