Amicon, Inc. - FDA 510(k) Cleared Devices
20
Total
20
Cleared
0
Denied
Amicon, Inc. has 20 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 20 cleared submissions from 1976 to 1993. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Amicon, Inc. Filter by specialty or product code using the sidebar.
20 devices
Cleared
Aug 05, 1993
CENTRICON -50 CONCENTRATOR
Chemistry
204d
Cleared
Nov 01, 1990
AMICON DIAFILTER 30 HEMOCONCENTRATOR
Gastroenterology & Urology
126d
Cleared
May 18, 1990
AMICON HEMOCONCENTRATOR SET
Gastroenterology & Urology
59d
Cleared
Feb 16, 1990
CENTRIPREP 100
Chemistry
29d
Cleared
Jan 11, 1990
AMICON MINIFILTER PLUS HEMOFILTER
Gastroenterology & Urology
126d
Cleared
Jul 20, 1989
CENTRICON CONCENTRATOR
Chemistry
64d
Cleared
Jun 13, 1989
AMICON VITAFIBER FLO-PATH BIORECT/VLS CELL CULT SY
Pathology
62d
Cleared
Feb 19, 1988
AMICON EQUALINE FLUID BALANCE SYSTEM
Gastroenterology & Urology
66d
Cleared
Mar 19, 1987
CENTRIPREP CONCENTRATOR
Chemistry
28d
Cleared
Nov 06, 1986
AMICON DIAFILTER HEMOFILTER
Gastroenterology & Urology
37d
Cleared
Sep 12, 1985
MINIFILTER HEMOFILTER
Gastroenterology & Urology
22d
Cleared
Jan 30, 1984
CENTRICON MICRO-CONCENTRATOR
Chemistry
77d