FDA 510(k)

Bosley Revitalizer 272 激光帽，Bosley Revitalizer 164 激光杯

K号: K181253 · 2018-08-10

申请人Pjm Worldwide, LLC D/B/A Phoenix Medical Technology, LLC

决定日期2018-08-10

产品代码OAP

咨询委员会PM 请注意，由于您没有提供具体的医疗设备监管文本，我无法进行翻译。请提供具体的文本内容，以便我能够按照您的要求进行翻译。

决定实质等同

器械摘要

Bosley Revitalizer 272 Laser Cap, Bosley Revitalizer 164 Laser Cup is the device name listed in this FDA 510(k) record. The listed applicant is Pjm Worldwide, LLC D/B/A Phoenix Medical Technology, LLC. It received FDA 510(k) clearance on 2018-08-10 under 510(k) number K181253. The device is classified under product code OAP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Bosley Revitalizer 272 Laser Cap, Bosley Revitalizer 164 Laser Cup?

Bosley Revitalizer 272 Laser Cap, Bosley Revitalizer 164 Laser Cup is a medical device that received FDA 510(k) clearance on 2018-08-10. The listed applicant is Pjm Worldwide, LLC D/B/A Phoenix Medical Technology, LLC. The 510(k) number is K181253.

When did Bosley Revitalizer 272 Laser Cap, Bosley Revitalizer 164 Laser Cup receive FDA 510(k) clearance?

Bosley Revitalizer 272 Laser Cap, Bosley Revitalizer 164 Laser Cup received FDA 510(k) clearance on 2018-08-10, under 510(k) number K181253.

Who is the listed applicant for Bosley Revitalizer 272 Laser Cap, Bosley Revitalizer 164 Laser Cup?

The FDA 510(k) record lists Pjm Worldwide, LLC D/B/A Phoenix Medical Technology, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Bosley Revitalizer 272 Laser Cap, Bosley Revitalizer 164 Laser Cup?

The FDA product code for Bosley Revitalizer 272 Laser Cap, Bosley Revitalizer 164 Laser Cup is OAP.

列明Pjm Worldwide, LLC D/B/A Phoenix Medical Technology, LLC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。

K192585Bosley Revitalizer 96 激光帽，Bosley Revitalizer 96 XL 激光帽

相关器械（代码：OAP）

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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