# Erika, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 43 (1976–1985): 43 510(k) clearances
- Product codes: KOC (13), FJI (8), FHS (6), FJK (5), FKQ (2), KPO (2), FKX (1), FJG (1), FRN (1), FPA (1), KDC (1), KRO (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (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 Medical Care North America: 3 (https://510kreport.com/company/fresenius-medical-care-north-america)
- Kaybath, Inc.: 1 (https://510kreport.com/company/kaybath)

## Its most-cited devices
- K810925: Naturalyte Bicarbonate Dialysate Concen. (1981), cited by 2
- K852310: Naturalyte Bicarbonate Concentrate-Dry Pack (1985), cited by 1
- K823115: Naturalyte Bicarbonate Dialysate 4400 (1982), cited by 1

## Recent decisions
- K853134: National Med Care Infusion Pump Adm Set #95-0001-8 (Nov 6, 1985)
- K852310: Naturalyte Bicarbonate Concentrate-Dry Pack (Jul 26, 1985)
- K852309: Erika Art LI, 3-9621-8, 22-6, 23-4 & Ven 9714-1 (Jul 26, 1985)
- K850866: Toray Industries Filtryzer Hollow Fiber Kidney B1L (Apr 3, 1985)
- K850865: Toray Industries Filtryzer Hollow Fiber Kidney B1- (Apr 3, 1985)
- K850655: Toray Ind. Filtryzer Hollow Fiber Artif. Kidney B2 (Mar 7, 1985)
- K850654: Toray Indus. Filtryzer Hollow Fiber Artificial Kid (Mar 7, 1985)
- K842436: Erika Negative Press. Arterial Blood (Jul 13, 1984)

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