FDA 510(k)

Astroid 规劃應用程式

K 號：K173940 · 2018-05-15

決定日期2018-05-15

產品代碼MUJ

諮詢委員會RA

決定相當於

器材摘要

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.

常見問題

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.

其他以 .Decimal, LLC 為申請人之記錄

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K211511十進位針劑 K192554十進位3D

相關器械（代碼：MUJ）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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官方來源

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