Class Class II

Hidroxa SE30 (K241267)

K241267 2024-10-17 Traditional
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Description

Hidroxa SE30 by Hidroxa Medical AB, an FDA 510(k) cleared physical medicine device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241267
Clearance Date2024-10-17
Clearance TypeTraditional
Product CodeEGJ
Regulation Number890.5525

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