# Amicon, Inc.

- Location (FDA's records): Danvers, MA
- FDA decisions: 20 (1976–1993): 20 510(k) clearances
- Product codes: KDI (8), JJH (6), KPF (1), JRL (1), KJF (1), JQQ (1), JJP (1), DHX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Fresenius USA, Inc.: 1 (https://510kreport.com/company/fresenius-usa)

## Its most-cited devices
- K902837: Amicon Diafilter 30 Hemoconcentrator (1990), cited by 1

## Recent decisions
- K930168: Centricon -50 Concentrator (Aug 5, 1993)
- K902837: Amicon Diafilter 30 Hemoconcentrator (Nov 1, 1990)
- K901286: Amicon Hemoconcentrator Set (May 18, 1990)
- K900280: Centriprep 100 (Feb 16, 1990)
- K895405: Amicon Minifilter Plus Hemofilter (Jan 11, 1990)
- K893733: Centricon Concentrator (Jul 20, 1989)
- K892645: Amicon Vitafiber Flo-Path Biorect/VLS Cell Cult SY (Jun 13, 1989)
- K875121: Amicon Equaline Fluid Balance System (Feb 19, 1988)

Source page: https://510kreport.com/company/amicon