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FDA 510(k)

Philips Avent Comfort 单/双电动吸奶器

K号: K161532 · 2016-08-29

决定日期2016-08-29
产品代码HGX
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决定实质等同

器械摘要

Philips Avent Comfort Single/Twin Electric Breast Pump is the device name listed in this FDA 510(k) record. The listed applicant is Philips Consumer Lifestyle - Innovation Site Eindhoven. It received FDA 510(k) clearance on 2016-08-29 under 510(k) number K161532. The device is classified under product code HGX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Philips Avent Comfort Single/Twin Electric Breast Pump?

Philips Avent Comfort Single/Twin Electric Breast Pump is a medical device that received FDA 510(k) clearance on 2016-08-29. The listed applicant is Philips Consumer Lifestyle - Innovation Site Eindhoven. The 510(k) number is K161532.

When did Philips Avent Comfort Single/Twin Electric Breast Pump receive FDA 510(k) clearance?

Philips Avent Comfort Single/Twin Electric Breast Pump received FDA 510(k) clearance on 2016-08-29, under 510(k) number K161532.

Who is the listed applicant for Philips Avent Comfort Single/Twin Electric Breast Pump?

The FDA 510(k) record lists Philips Consumer Lifestyle - Innovation Site Eindhoven as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Philips Avent Comfort Single/Twin Electric Breast Pump?

The FDA product code for Philips Avent Comfort Single/Twin Electric Breast Pump is HGX.

相关临床试验

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列明Philips Consumer Lifestyle - Innovation Site Eindhoven为申报人的其他记录

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相关器械(代码:HGX)

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。

官方来源

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