FDA 510(k)

L- OVC (注意：原文中未提供具体内容，因此无法进行翻译。请提供完整的设备名称或文本内容以便进行翻译。)

K 號：K162677 · 2016-12-21

決定日期2016-12-21

產品代碼EIH

諮詢委員會DE

決定相當於

器材摘要

L- OVC is the device name listed in this FDA 510(k) record. The listed applicant is Rhondium, Ltd.. It received FDA 510(k) clearance on 2016-12-21 under 510(k) number K162677. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the L- OVC?

L- OVC is a medical device that received FDA 510(k) clearance on 2016-12-21. The listed applicant is Rhondium, Ltd.. The 510(k) number is K162677.

When did L- OVC receive FDA 510(k) clearance?

L- OVC received FDA 510(k) clearance on 2016-12-21, under 510(k) number K162677.

Who is the listed applicant for L- OVC?

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

What is the FDA product code for L- OVC?

The FDA product code for L- OVC is EIH.

相關器械（代碼：EIH）

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