Class Class II

Magic InBra (K251377)

K251377 2025-09-18 Traditional
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Description

Magic InBra by Medela AG, an FDA 510(k) cleared obstetrics/gynecology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251377
Clearance Date2025-09-18
Clearance TypeTraditional
Product CodeHGX
Regulation Number884.5160

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