FDA 510(k)

第一緩解 v1

K 號：K202940 · 2020-12-29

決定日期2020-12-29

產品代碼QHH

諮詢委員會GU

決定相當於

器材摘要

First Relief v1 is the device name listed in this FDA 510(k) record. The listed applicant is Dyansys, Inc.. It received FDA 510(k) clearance on 2020-12-29 under 510(k) number K202940. The device is classified under product code QHH. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the First Relief v1?

First Relief v1 is a medical device that received FDA 510(k) clearance on 2020-12-29. The listed applicant is Dyansys, Inc.. The 510(k) number is K202940.

When did First Relief v1 receive FDA 510(k) clearance?

First Relief v1 received FDA 510(k) clearance on 2020-12-29, under 510(k) number K202940.

Who is the listed applicant for First Relief v1?

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

What is the FDA product code for First Relief v1?

The FDA product code for First Relief v1 is QHH.

其他以 Dyansys, Inc. 為申請人之記錄

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相關器械（代碼：QHH）

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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