FDA 510(k)

Raycell Mk2

K号: K161324 · 2016-08-12

决定日期2016-08-12

产品代码MOT

决定实质等同

器械摘要

Raycell Mk2 is the device name listed in this FDA 510(k) record. The listed applicant is Best Theratronics Limited. It received FDA 510(k) clearance on 2016-08-12 under 510(k) number K161324. The device is classified under product code MOT. FDA Decision: Substantially Equivalent.

常见问题

What is the Raycell Mk2?

Raycell Mk2 is a medical device that received FDA 510(k) clearance on 2016-08-12. The listed applicant is Best Theratronics Limited. The 510(k) number is K161324.

When did Raycell Mk2 receive FDA 510(k) clearance?

Raycell Mk2 received FDA 510(k) clearance on 2016-08-12, under 510(k) number K161324.

Who is the listed applicant for Raycell Mk2?

The FDA 510(k) record lists Best Theratronics Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Raycell Mk2?

The FDA product code for Raycell Mk2 is MOT.

列明Best Theratronics Limited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。

K181737Raycell MK1

官方来源

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