Class Class II

Philips Lumea IPL (K253754)

K253754 2025-12-23 Special
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Description

Philips Lumea IPL by Philips Consumer Lifestyle B.V., an FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK253754
Clearance Date2025-12-23
Clearance TypeSpecial
Product CodeOHT
Regulation Number878.4810

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