# Sabratek Corp.

- Location (FDA's records): Niles, IL
- FDA decisions: 7 (1992–1999): 7 510(k) clearances
- Product codes: FRN (4), FLL (1), MHX (1), FPA (1)
- Predicates its devices cite: 7 (2 its own); citations of its devices by later devices: 6 (2 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Diatek, Inc.: 1 (https://510kreport.com/company/diatek)
- Protocol Systems, Inc.: 1 (https://510kreport.com/company/protocol-systems)
- Pro-Tech Services, Inc.: 1 (https://510kreport.com/company/pro-tech-services)
- Lead-Lok, Inc.: 1 (https://510kreport.com/company/lead-lok)
- A&D Engineering, Inc.: 1 (https://510kreport.com/company/a-d-engineering)

## Firms that cite its devices most
- Alaris Medical Systems, Inc.: 1 (https://510kreport.com/company/alaris-medical-systems)
- Alexander Mfg. Co.: 1 (https://510kreport.com/company/alexander-mfg)
- Becton Dickinson Curlin, LLC: 1 (https://510kreport.com/company/becton-dickinson-curlin)
- Nexan Telemed, Ltd.: 1 (https://510kreport.com/company/nexan-telemed)

## Its most-cited devices
- K941984: Sabratek 6060 Homerun Volumetric Infusion Pump (1994), cited by 3
- K914589: Sabratek 3030 Infusion Pump (1992), cited by 2
- K980619: Sabratek Patient Home Management System (1998), cited by 1

## Recent decisions
- K983355: Sabratek Apm-2000 Ambulatory Patient Montor, Transcutaneous Temperature Monitor (Mar 12, 1999)
- K980751: Sabratek 4040 Infusion Pump (Feb 24, 1999)
- K980619: Sabratek Patient Home Management System (Aug 20, 1998)
- K955258: 3030 Infusion Pump (Jun 3, 1996)
- K944293: Sabratek Sabsil Sets (Mar 23, 1995)
- K941984: Sabratek 6060 Homerun Volumetric Infusion Pump (Jul 19, 1994)
- K914589: Sabratek 3030 Infusion Pump (May 18, 1992)

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