Philips Lumea IPL— 510(k) K253754
Substantially EquivalentPhilips Consumer Lifestyle B.V.
FDA 510(k) clearance K253754 for Philips Lumea IPL, Substantially Equivalent on 2025-12-23. Applicant: Philips Consumer Lifestyle B.V.. Device class: 2.
Clearance details
- Applicant
- Philips Consumer Lifestyle B.V.
- Product code
- Code OHT
- Device class
- Class 2
- Regulation
- 21 CFR 878.4810
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Drachten, NL
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More clearances from Philips Consumer Lifestyle B.V.
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