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FDA 510(k)

Philips Avent Single/Double electric breast pump Advanced

K-Number: K201381 · 2020-10-01

Decision Date2020-10-01
Product CodeHGX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Philips Avent Single/Double electric breast pump Advanced is a medical device manufactured by Philips Consumer Lifestyle - Innovation Site Eindhoven. It received FDA 510(k) clearance on 2020-10-01 under approval number K201381. The device is classified under product code HGX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.