510(k) K251377

Magic InBra by Medela AG — Product Code HGX

K251377 is an FDA 510(k) premarket notification submitted by Medela AG for the device "Magic InBra". The FDA issued a decision of Substantially Equivalent on September 18, 2025. The device falls under product code HGX (Pump, Breast, Powered), a Class II device regulated under 21 CFR 884.5160. Medela AG has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 18, 2025
Date Received
May 2, 2025
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Pump, Breast, Powered
Device Class
Class II
Regulation Number
884.5160
Review Panel
OB
Submission Type