# Philips India Limited

- Location (FDA's records): Pune, IN
- FDA decisions: 2 (2017–2021): 2 510(k) clearances
- Product codes: IZL (1), OWB (1)
- Predicates its devices cite: 2 (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
- Sedecal., Sa.: 1 (https://510kreport.com/company/sedecal)
- Philips Medical Systems Nederland B.V.: 1 (https://510kreport.com/company/philips-medical-systems-nederland)

## Recent decisions
- K203623: StentBoost Mobile (Apr 5, 2021)
- K173187: MobileDiagnost M50 (Nov 16, 2017)

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