510(k) K212773

ARDO Alyssa by Ardo Medical AG — Product Code HGX

K212773 is an FDA 510(k) premarket notification submitted by Ardo Medical AG for the device "ARDO Alyssa". The FDA issued a decision of Substantially Equivalent on Apr 15, 2022. The device falls under product code HGX (Pump, Breast, Powered), a Class II device regulated under 21 CFR 884.5160. Ardo Medical AG has 5 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Apr 15, 2022
Date Received
Aug 31, 2021
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
510(k)