FDA 510(k)

Hang&Go 製備醫療設備規範文本

K 號：K161613 · 2016-12-28

決定日期2016-12-28

產品代碼LGZ

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

Hang&Go PAC is the device name listed in this FDA 510(k) record. The listed applicant is Rand S.R.L.. It received FDA 510(k) clearance on 2016-12-28 under 510(k) number K161613. The device is classified under product code LGZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Hang&Go PAC?

Hang&Go PAC is a medical device that received FDA 510(k) clearance on 2016-12-28. The listed applicant is Rand S.R.L.. The 510(k) number is K161613.

When did Hang&Go PAC receive FDA 510(k) clearance?

Hang&Go PAC received FDA 510(k) clearance on 2016-12-28, under 510(k) number K161613.

Who is the listed applicant for Hang&Go PAC?

The FDA 510(k) record lists Rand S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Hang&Go PAC?

The FDA product code for Hang&Go PAC is LGZ.

相關器械（代碼：LGZ）

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官方來源

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