FDA 510(k)

Beurer IPL 8500 设备/ IPL VelvetSkin Pro

K号: K181734 · 2018-09-19

决定日期2018-09-19

产品代码OHT

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决定实质等同

器械摘要

Beurer IPL 8500 device/ IPL VelvetSkin Pro is the device name listed in this FDA 510(k) record. The listed applicant is Home Well Trading, Ltd.. It received FDA 510(k) clearance on 2018-09-19 under 510(k) number K181734. The device is classified under product code OHT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Beurer IPL 8500 device/ IPL VelvetSkin Pro?

Beurer IPL 8500 device/ IPL VelvetSkin Pro is a medical device that received FDA 510(k) clearance on 2018-09-19. The listed applicant is Home Well Trading, Ltd.. The 510(k) number is K181734.

When did Beurer IPL 8500 device/ IPL VelvetSkin Pro receive FDA 510(k) clearance?

Beurer IPL 8500 device/ IPL VelvetSkin Pro received FDA 510(k) clearance on 2018-09-19, under 510(k) number K181734.

Who is the listed applicant for Beurer IPL 8500 device/ IPL VelvetSkin Pro?

The FDA 510(k) record lists Home Well Trading, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Beurer IPL 8500 device/ IPL VelvetSkin Pro?

The FDA product code for Beurer IPL 8500 device/ IPL VelvetSkin Pro is OHT.

列明Home Well Trading, Ltd.为申报人的其他记录

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。

K181121Beurer IPL 5500 设备/ IPL 5000/ IPL PureSkin Pro

相关器械（代码：OHT）

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。

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