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FDA 510(k)

完美LED紅外線設備

K 號:K152332 · 2016-02-25

決定日期2016-02-25
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

Perfectio LED infrared device is the device name listed in this FDA 510(k) record. The listed applicant is Omm Imports Inc Dba Zero Gravity. It received FDA 510(k) clearance on 2016-02-25 under 510(k) number K152332. 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 Perfectio LED infrared device?

Perfectio LED infrared device is a medical device that received FDA 510(k) clearance on 2016-02-25. The listed applicant is Omm Imports Inc Dba Zero Gravity. The 510(k) number is K152332.

When did Perfectio LED infrared device receive FDA 510(k) clearance?

Perfectio LED infrared device received FDA 510(k) clearance on 2016-02-25, under 510(k) number K152332.

Who is the listed applicant for Perfectio LED infrared device?

The FDA 510(k) record lists Omm Imports Inc Dba Zero Gravity as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Perfectio LED infrared device?

The FDA product code for Perfectio LED infrared device is OHS.

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相關器械(代碼:OHS)

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。

官方來源

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