Class Class II

Philips Lumea IPL (K243453)

K243453 2025-02-10 Traditional
Home/ Devices/ Philips Lumea IPL (K243453)

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) NumberK243453
Clearance Date2025-02-10
Clearance TypeTraditional
Product CodeOHT
Regulation Number878.4810

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