# Philips Int'L B.V.

- Location (FDA's records): The Netherlands, NL
- FDA decisions: 11 (1985–1992): 11 510(k) clearances
- Product codes: FTC (9), ESD (2)
- Predicates its devices cite: 0 (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

## Recent decisions
- K920134: Philips 41 Series Rainbow (Jan 24, 1992)
- K920142: Philips M60 Series (Jan 23, 1992)
- K852348: Philips Solarium HP 3134 (Jun 27, 1985)
- K851535: Philips UV-a Solarium Type HP 3140 (May 1, 1985)
- K851536: Philips UV-a Solarium Type HP 3141 (May 1, 1985)
- K851533: Philips UV-a Sdarium Type HP 3148(CFR 21 Sunlamp (May 1, 1985)
- K851534: Philips UV-a Solarium Type HP 3150 (May 1, 1985)
- K850206: Philips UV-a Solarium Type HP 3126-Sunlamp (Feb 21, 1985)

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