# Philips Electronics UK Limited

- Location (FDA's records): Glemsford, Suffolk, GB
- FDA decisions: 3 (2009–2010): 3 510(k) clearances
- Product codes: FLL (1), KKO (1), HGY (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 0 (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 whose devices it cites most
- Burditt & Calkins-Siemens-Elema: 1 (https://510kreport.com/company/burditt-calkins-siemens-elema)
- Avent America, Inc.: 1 (https://510kreport.com/company/avent-america)
- Medela AG: 1 (https://510kreport.com/company/medela)

## Recent decisions
- K101538: Handheld Manual Breast Pump (Avent Manual Breast Pump) (Nov 5, 2010)
- K100495: Philips Avent Digital Thermometer Set, Model SCH540 (Jun 22, 2010)
- K090167: Philips Avent Classic Stage 2 and 3 Teether, Model SCF882/01, SCF884/01, Philips Avent Animal Stage 2 and 3 Teether, (Jun 18, 2009)

Source page: https://510kreport.com/company/philips-electronics-uk