FDA 510(k)

Synergy Marble (型號：Opasm)

K 號：K220064 · 2022-07-22

決定日期2022-07-22

產品代碼OHS

諮詢委員會SU 請提供完整的描述文本，以便我進行翻譯。

決定相當於

器材摘要

Synergy Marble (Model: Opasm) is the device name listed in this FDA 510(k) record. The listed applicant is Yrs Group, Inc.. It received FDA 510(k) clearance on 2022-07-22 under 510(k) number K220064. The device is classified under product code OHS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Synergy Marble (Model: Opasm)?

Synergy Marble (Model: Opasm) is a medical device that received FDA 510(k) clearance on 2022-07-22. The listed applicant is Yrs Group, Inc.. The 510(k) number is K220064.

When did Synergy Marble (Model: Opasm) receive FDA 510(k) clearance?

Synergy Marble (Model: Opasm) received FDA 510(k) clearance on 2022-07-22, under 510(k) number K220064.

Who is the listed applicant for Synergy Marble (Model: Opasm)?

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

What is the FDA product code for Synergy Marble (Model: Opasm)?

The FDA product code for Synergy Marble (Model: Opasm) is OHS.

其他以 Yrs Group, Inc. 為申請人之記錄

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K210954協和

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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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