Class Class II

BELLUS-Q (K253344)

K253344 2025-11-25 Traditional
Home/ Devices/ BELLUS-Q (K253344)

Description

BELLUS-Q by Speclipse, Inc., an FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK253344
Clearance Date2025-11-25
Clearance TypeTraditional
Product CodeGEX
Regulation Number878.4810

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