Medisystems Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medisystems Corp. - FDA 510(k) Cleared Devices
22
Total
22
Cleared
0
Denied
Medisystems Corp. has 22 FDA 510(k) cleared gastroenterology & urology devices. Based in Mchenry, US.
Historical record: 22 cleared submissions from 1981 to 2007.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medisystems Corp.
22 devices
Cleared
Feb 12, 2007
MEDISYSTEMS ARTERIAL-VENOUS FISTULA NEEDLE SET WITH SECUREMENT DEVICE
Gastroenterology & Urology
136d
Cleared
May 29, 2001
MEDISYSTEMS LUER ACCESS INJECTION SITE
General Hospital
119d
Cleared
Oct 25, 2000
ACCESS ALERT GAUGE
Gastroenterology & Urology
82d
Cleared
Mar 20, 2000
REVERSO
Gastroenterology & Urology
90d
Cleared
Jan 06, 2000
MEDISYSTEMS BUTTONHOLE NEEDLE SETS
Gastroenterology & Urology
302d
Cleared
Nov 25, 1998
MEDISYSTEMS TRANSDUCER PROTECTOR
Gastroenterology & Urology
84d
Cleared
Aug 18, 1997
MEDISYSTEMS DIALYSIS PRIMING SETS
Gastroenterology & Urology
90d
Cleared
Aug 15, 1997
MEDISYSTEMS PERITONEAL DIALYSIS SETS
Gastroenterology & Urology
336d
Cleared
May 12, 1997
MEDISYSTEMS TRANDUCER PROTECTOR
Gastroenterology & Urology
89d
Cleared
Sep 23, 1996
ARTERIAL VENOUS BLOOD TUBING SET
Gastroenterology & Urology
405d
Cleared
Feb 18, 1994
MEDISYSTEMS APHERESIS NEEDLE WITH GUARD
Gastroenterology & Urology
296d
Cleared
Jun 20, 1991
MEDISYSTEMS HEMODIALYSIS FISTULA SET
Gastroenterology & Urology
119d