FDA 510(k)

Sporview VH202 医療設備規範文本

K 號：K171287 · 2018-02-01

申請人Spsmedical Supply Corp. A Division of Cantel Medical

決定日期2018-02-01

產品代碼FRC

諮詢委員會醫療設備規範文本翻譯如下： HO 注意：原文中未提供具體的醫療設備規範文本，因此上述翻譯僅為示例。請提供完整的規範文本以便進行準確翻譯。

決定相當於

器材摘要

Sporview VH202 BI is the device name listed in this FDA 510(k) record. The listed applicant is Spsmedical Supply Corp. A Division of Cantel Medical. It received FDA 510(k) clearance on 2018-02-01 under 510(k) number K171287. The device is classified under product code FRC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Sporview VH202 BI?

Sporview VH202 BI is a medical device that received FDA 510(k) clearance on 2018-02-01. The listed applicant is Spsmedical Supply Corp. A Division of Cantel Medical. The 510(k) number is K171287.

When did Sporview VH202 BI receive FDA 510(k) clearance?

Sporview VH202 BI received FDA 510(k) clearance on 2018-02-01, under 510(k) number K171287.

Who is the listed applicant for Sporview VH202 BI?

The FDA 510(k) record lists Spsmedical Supply Corp. A Division of Cantel Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Sporview VH202 BI?

The FDA product code for Sporview VH202 BI is FRC.

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器材摘要

常見問題

相關臨床試驗

相關器械（代碼：FRC）

官方來源