Philips Avent Single/Double electric breast pump Advanced
K-Number: K201381 · 2020-10-01
Device Summary
Frequently Asked Questions
What is the Philips Avent Single/Double electric breast pump Advanced?
Philips Avent Single/Double electric breast pump Advanced is a medical device that received FDA 510(k) clearance on 2020-10-01. It is manufactured by Philips Consumer Lifestyle - Innovation Site Eindhoven. The 510(k) number is K201381.
When was Philips Avent Single/Double electric breast pump Advanced approved by the FDA?
Philips Avent Single/Double electric breast pump Advanced received FDA 510(k) clearance on 2020-10-01, under approval number K201381.
What company makes Philips Avent Single/Double electric breast pump Advanced?
Philips Avent Single/Double electric breast pump Advanced is manufactured by Philips Consumer Lifestyle - Innovation Site Eindhoven.
What is the FDA product code for Philips Avent Single/Double electric breast pump Advanced?
The FDA product code for Philips Avent Single/Double electric breast pump Advanced is HGX.
Related Clinical Trials
Other Devices by Philips Consumer Lifestyle - Innovation Site Eindhoven
Related Devices (Code: HGX)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.