510(k) K161532

Philips Avent Comfort Single/Twin Electric Breast Pump by Philips Consumer Lifestyle - Innovation Site Eindhoven — Product Code HGX

K161532 is an FDA 510(k) premarket notification submitted by Philips Consumer Lifestyle - Innovation Site Eindhoven for the device "Philips Avent Comfort Single/Twin Electric Breast Pump". The FDA issued a decision of Substantially Equivalent on Aug 29, 2016. 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
Aug 29, 2016
Date Received
Jun 2, 2016
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)