# Phillips Medical Systems

- Location (FDA's records): Andover, MA
- FDA decisions: 4 (2004–2015): 4 510(k) clearances
- Product codes: DSJ (1), IYN (1), MHX (1), MWI (1)
- Predicates its devices cite: 7 (0 its own); citations of its devices by later devices: 5 (0 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
- Philips Medical Systems, Inc.: 4 (https://510kreport.com/company/philips-medical-systems)
- Philips Medizin Systeme Boeblingen GmbH: 2 (https://510kreport.com/company/philips-medizin-systeme-boeblingen)
- Philips Medizinsysteme Boeblingen GmbH, Cardiac AN: 1 (https://510kreport.com/company/philips-medizinsysteme-boeblingen-cardiac-an)

## Firms that cite its devices most
- Philips Medical Systems, Inc.: 3 (https://510kreport.com/company/philips-medical-systems)
- Philips Medizin Systeme Boeblingen GmbH: 1 (https://510kreport.com/company/philips-medizin-systeme-boeblingen)
- Therapeutic Monitoring Systems (Tms), Inc.: 1 (https://510kreport.com/company/therapeutic-monitoring-systems-tms)

## Its most-cited devices
- K103646: Intellivue MX40 Patient Monitor (2011), cited by 3
- K151761: SureSigns VS3, SureSigns VS4 (2015), cited by 2

## Recent decisions
- K151761: SureSigns VS3, SureSigns VS4 (Sep 29, 2015)
- K103646: Intellivue MX40 Patient Monitor (Jan 7, 2011)
- K080548: HD7 Diagnostic Ultrasound System (Mar 27, 2008)
- K041942: M2376A Devicelink System (Jul 23, 2004)

Source page: https://510kreport.com/company/phillips-medical-systems