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Amicon, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
20
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K930168CENTRICON -50 CONCENTRATORAugust 5, 1993
K902837AMICON DIAFILTER 30 HEMOCONCENTRATORNovember 1, 1990
K901286AMICON HEMOCONCENTRATOR SETMay 18, 1990
K900280CENTRIPREP 100February 16, 1990
K895405AMICON MINIFILTER PLUS HEMOFILTERJanuary 11, 1990
K893733CENTRICON CONCENTRATORJuly 20, 1989
K892645AMICON VITAFIBER FLO-PATH BIORECT/VLS CELL CULT SYJune 13, 1989
K875121AMICON EQUALINE FLUID BALANCE SYSTEMFebruary 19, 1988
K870690CENTRIPREP CONCENTRATORMarch 19, 1987
K863823AMICON DIAFILTER HEMOFILTERNovember 6, 1986
K853510MINIFILTER HEMOFILTERSeptember 12, 1985
K833919CENTRICON MICRO-CONCENTRATORJanuary 30, 1984
K823881ARTERIOVENOUS BLOOD TUBING SET FORJanuary 17, 1983
K823288AMICON DIAFILTERS 20 & 30 HEMOFILTERSDecember 16, 1982
K813591HEMOFILTERSMarch 31, 1982
K820455CENTRIFREE MICROPARTITION SYSTEMMarch 15, 1982
K810810AMICON ULTRAFILTRATION MEMBRANES CMIIApril 17, 1981
K770398MINICONApril 6, 1977
K761100MULTI-CELL ULTRAFILTRATION SYSTEMDecember 6, 1976
K760592MINICON CONCENTRATORNovember 23, 1976