510(k) K172772

Freemie Independence, Freemie Liberty by Dao Health — Product Code HGX

K172772 is an FDA 510(k) premarket notification submitted by Dao Health for the device "Freemie Independence, Freemie Liberty". The FDA issued a decision of Substantially Equivalent on Oct 13, 2017. The device falls under product code HGX (Pump, Breast, Powered), a Class II device regulated under 21 CFR 884.5160. Dao Health has 2 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Oct 13, 2017
Date Received
Sep 14, 2017
Clearance Type
Traditional
Expedited Review
No
Third Party Review
Yes

Device Classification

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