Seratronics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Seratronics, Inc. - FDA 510(k) Cleared Devices
21
Total
21
Cleared
0
Denied
Seratronics, Inc. has 21 FDA 510(k) cleared gastroenterology & urology devices. Based in Mchenry, US.
Historical record: 21 cleared submissions from 1982 to 1996.
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 - Seratronics, Inc.
21 devices
Cleared
Oct 21, 1996
DPS 4 DIALYZER PREPARATION SYSTEM
Gastroenterology & Urology
336d
Cleared
Apr 18, 1996
DRS 4 DIALYZER REPROCESSING SYSTEM
Gastroenterology & Urology
1129d
Cleared
Nov 29, 1995
DRS 4 ND DIALYZER REPROCESSING SYSTEM
Gastroenterology & Urology
440d
Cleared
Aug 29, 1994
DMS DATA MANAGEMENT SYSTEM/DRS-4 DIALYZER REPROCES
Gastroenterology & Urology
774d
Cleared
Feb 24, 1992
DRS-4 DIALYZER REPROCESSING SYSTEM
Gastroenterology & Urology
131d
Cleared
Apr 25, 1988
FRESENIUS PURISTERIL 340 (TM)
Gastroenterology & Urology
172d
Cleared
Feb 19, 1988
FRESENIUS HEMOFLOW F3, F4, F5, F7
Gastroenterology & Urology
84d
Cleared
May 01, 1987
FRESENIUS HEMOFLOW F6 AND F8
Gastroenterology & Urology
66d
Cleared
Apr 01, 1987
FRESENIUS HEMOFLOW F60 AND F80
Gastroenterology & Urology
36d
Cleared
Mar 03, 1987
FRESENIUS ULTRAFLUX AV400, AV600
Gastroenterology & Urology
102d
Cleared
Nov 06, 1986
FRESENIUS HEMOFLOW F50 & F70
Gastroenterology & Urology
13d
Cleared
Apr 07, 1986
DRS-4 DIALYZER REPROCESSING SYSTEM
Gastroenterology & Urology
42d