510(k) K203383

Philips Avent Double electric breast pump Advanced SCF394/61, Philips Avent Double electric breast pump Advanced SCF394/62 by Philips Consumer Lifestyle - Innovation Site Eindhoven — Product Code HGX

K203383 is an FDA 510(k) premarket notification submitted by Philips Consumer Lifestyle - Innovation Site Eindhoven for the device "Philips Avent Double electric breast pump Advanced SCF394/61, Philips Avent Double electric breast pump Advanced SCF394/62". The FDA issued a decision of Substantially Equivalent on Dec 15, 2020. The device falls under product code HGX (Pump, Breast, Powered), a Class II device regulated under 21 CFR 884.5160. Philips Consumer Lifestyle - Innovation Site Eindhoven has 2 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Dec 15, 2020
Date Received
Nov 17, 2020
Clearance Type
Special
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)