# Seratronics, Inc.

- Location (FDA's records): Concord, CA
- FDA decisions: 21 (1982–1996): 21 510(k) clearances
- Product codes: LIF (9), KDI (6), FJI (2), FKQ (2), FLC (1), FJK (1)
- Predicates its devices cite: 1 (1 its own); citations of its devices by later devices: 9 (1 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Novaflux Technologies: 3 (https://510kreport.com/company/novaflux-technologies)
- Fresenius Medical Care Renal Therapies Group, LLC: 1 (https://510kreport.com/company/fresenius-medical-care-renal-therapies-group)
- Althin Medical AB an Affiliate of Baxter Intl: 1 (https://510kreport.com/company/althin-medical-ab-an-affiliate-of-baxter-intl)
- Bioteque Corp.: 1 (https://510kreport.com/company/bioteque)
- Dynamic Technology Corp.: 1 (https://510kreport.com/company/dynamic-technology)
- Alcavis International, Inc.: 1 (https://510kreport.com/company/alcavis-international)

## Its most-cited devices
- K860674: DRS-4 Dialyzer Reprocessing System (1986), cited by 2
- K914580: DRS-4 Dialyzer Reprocessing System (1992), cited by 1
- K931336: DRS 4 Dialyzer Reprocessing System (1996), cited by 1
- K874872: Fresenius Hemoflow F3, F4, F5, F7 (1988), cited by 1
- K852251: Fresenius Hemoflow F60 & Fresenius Hemoflow F40 (1985), cited by 1
- K832230: Dialyzer Preparation Sys DPS-4 (1983), cited by 1

## Recent decisions
- K955299: DPS 4 Dialyzer Preparation System (Oct 21, 1996)
- K931336: DRS 4 Dialyzer Reprocessing System (Apr 18, 1996)
- K944539: DRS 4 ND Dialyzer Reprocessing System (Nov 29, 1995)
- K923529: DMS Data Management System/DRS-4 Dialyzer Reproces (Aug 29, 1994)
- K914580: DRS-4 Dialyzer Reprocessing System (Feb 24, 1992)
- K874573: Fresenius Puristeril 340 (TM) (Apr 25, 1988)
- K874872: Fresenius Hemoflow F3, F4, F5, F7 (Feb 19, 1988)
- K870725: Fresenius Hemoflow F6 and F8 (May 1, 1987)

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