Amicon, Inc.
Amicon, Inc. holds FDA 510(k) medical device clearances, first cleared 1976, most recent 1993.
Top product codes for Amicon, Inc.
Recent clearances by Amicon, Inc.
- K930168 — CENTRICON -50 CONCENTRATOR
- K902837 — AMICON DIAFILTER 30 HEMOCONCENTRATOR
- K901286 — AMICON HEMOCONCENTRATOR SET
- K900280 — CENTRIPREP 100
- K895405 — AMICON MINIFILTER PLUS HEMOFILTER
- K893733 — CENTRICON CONCENTRATOR
- K892645 — AMICON VITAFIBER FLO-PATH BIORECT/VLS CELL CULT SY
- K875121 — AMICON EQUALINE FLUID BALANCE SYSTEM
- K870690 — CENTRIPREP CONCENTRATOR
- K863823 — AMICON DIAFILTER HEMOFILTER
- K853510 — MINIFILTER HEMOFILTER
- K833919 — CENTRICON MICRO-CONCENTRATOR
- K823881 — ARTERIOVENOUS BLOOD TUBING SET FOR
- K823288 — AMICON DIAFILTERS 20 & 30 HEMOFILTERS
- K813591 — HEMOFILTERS
- K820455 — CENTRIFREE MICROPARTITION SYSTEM
- K810810 — AMICON ULTRAFILTRATION MEMBRANES CMII
- K770398 — MINICON
- K761100 — MULTI-CELL ULTRAFILTRATION SYSTEM
- K760592 — MINICON CONCENTRATOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.