# Philips Medical Systems Technologies, Ltd.

- Location (FDA's records): Haifa, IL
- FDA decisions: 5 (2018–2026): 5 510(k) clearances
- Names in FDA's records: Philips Medical Systems Technologies , Ltd. (4); Philips Medical Systems Technologies (1)
- Product codes: JAK (3), LLZ (2)
- 510(k) review time since 2016: median 127 days, against 141 for FDA's reviews in the same codes and years (3 of 5 faster)
- Predicates its devices cite: 7 (2 its own); citations of its devices by later devices: 4 (2 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Philips Medical Systems Nederland B.V.: 3 (https://510kreport.com/company/philips-medical-systems-nederland)
- Philips Medical Systems (Cleveland), Inc.: 1 (https://510kreport.com/company/philips-medical-systems-cleveland)
- Carestream Health, Inc.: 1 (https://510kreport.com/company/carestream-health)

## Firms that cite its devices most
- Philips Medical Systems Nederland B.V.: 1 (https://510kreport.com/company/philips-medical-systems-nederland)
- Philips Healthcare (Suzhou) Co., Ltd.: 1 (https://510kreport.com/company/philips-healthcare-suzhou)

## Its most-cited devices
- K240844: Spectral CT 7500 RT (2024), cited by 3
- K173588: Illumeo System (2018), cited by 1

## Recent decisions
- K253649: Spectral CT Verida Family (Mar 27, 2026)
- K244008: Spectral CT (May 16, 2025)
- K240844: Spectral CT 7500 RT (Oct 18, 2024)
- K240822: Image Management V15 (Apr 24, 2024)
- K173588: Illumeo System (Jan 12, 2018)

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