Philips Avent Double electric breast pump Advanced SCF394/61, Philips Avent Double electric breast pump Advanced SCF394/62
K-Number: K203383 · 2020-12-15
Device Summary
Frequently Asked Questions
What is the Philips Avent Double electric breast pump Advanced SCF394/61, Philips Avent Double electric breast pump Advanced SCF394/62?
Philips Avent Double electric breast pump Advanced SCF394/61, Philips Avent Double electric breast pump Advanced SCF394/62 is a medical device that received FDA 510(k) clearance on 2020-12-15. It is manufactured by Philips Consumer Lifestyle - Innovation Site Eindhoven. The 510(k) number is K203383.
When was Philips Avent Double electric breast pump Advanced SCF394/61, Philips Avent Double electric breast pump Advanced SCF394/62 approved by the FDA?
Philips Avent Double electric breast pump Advanced SCF394/61, Philips Avent Double electric breast pump Advanced SCF394/62 received FDA 510(k) clearance on 2020-12-15, under approval number K203383.
What company makes Philips Avent Double electric breast pump Advanced SCF394/61, Philips Avent Double electric breast pump Advanced SCF394/62?
Philips Avent Double electric breast pump Advanced SCF394/61, Philips Avent Double electric breast pump Advanced SCF394/62 is manufactured by Philips Consumer Lifestyle - Innovation Site Eindhoven.
What is the FDA product code for Philips Avent Double electric breast pump Advanced SCF394/61, Philips Avent Double electric breast pump Advanced SCF394/62?
The FDA product code for Philips Avent Double electric breast pump Advanced SCF394/61, Philips Avent Double electric breast pump Advanced SCF394/62 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.