FDA 510(k)

Astroid 规划应用

K号: K173940 · 2018-05-15

决定日期2018-05-15

产品代码MUJ

咨询委员会RA

决定实质等同

器械摘要

Astroid Planning App is the device name listed in this FDA 510(k) record. The listed applicant is .Decimal, LLC. It received FDA 510(k) clearance on 2018-05-15 under 510(k) number K173940. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Astroid Planning App?

Astroid Planning App is a medical device that received FDA 510(k) clearance on 2018-05-15. The listed applicant is .Decimal, LLC. The 510(k) number is K173940.

When did Astroid Planning App receive FDA 510(k) clearance?

Astroid Planning App received FDA 510(k) clearance on 2018-05-15, under 510(k) number K173940.

Who is the listed applicant for Astroid Planning App?

The FDA 510(k) record lists .Decimal, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Astroid Planning App?

The FDA product code for Astroid Planning App is MUJ.

列明.Decimal, 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。

K211511十进制推注 K192554十进制3D

官方来源

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