510(k) K150476

Spectra S1Plus and Spectra S2 Plus by Uzinmedicare Co. — Product Code HGX

K150476 is an FDA 510(k) premarket notification submitted by Uzinmedicare Co. for the device "Spectra S1Plus and Spectra S2 Plus". The FDA issued a decision of Substantially Equivalent on Apr 15, 2016. The device falls under product code HGX (Pump, Breast, Powered), a Class II device regulated under 21 CFR 884.5160. Uzinmedicare Co. has 6 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Apr 15, 2016
Date Received
Feb 24, 2015
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)