Sartorius Filters, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sartorius Filters, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Sartorius Filters, Inc. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 8 cleared submissions from 1982 to 1985.
Browse the FDA 510(k) cleared devices submitted by Sartorius Filters, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sartorius Filters, Inc.
8 devices
Cleared
Aug 19, 1985
SARTORIUS MINISART FH 16534
General Hospital
115d
Cleared
Aug 19, 1985
SARTORIUS MINI-SART FH 16555
General Hospital
115d
Cleared
Aug 19, 1985
SARTORIUS MINI SART FH 16592
General Hospital
115d
Cleared
Jun 04, 1985
SARTORIUS AQUASART SM 40035 - DIALYSATE SYS
Gastroenterology & Urology
120d
Cleared
Jan 18, 1985
SARTORIUS MINISART SM 16596HY
Gastroenterology & Urology
59d
Cleared
Apr 28, 1983
HEMO-PROCESSING SYSTEM
Gastroenterology & Urology
72d
Cleared
Nov 27, 1982
SARTOPHOR SYSTEM FOR ELECTROPHORESIS
Chemistry
33d
Cleared
Sep 21, 1982
CELLULOSE ACETATE MEMBRANE STRIPS
Chemistry
53d