熱痛專家
K 號：K181992 · 2018-11-09
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器材摘要
Heat Pain Pro is the device name listed in this FDA 510(k) record. The listed applicant is Omron Healthcare, Inc.. It received FDA 510(k) clearance on 2018-11-09 under 510(k) number K181992. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Heat Pain Pro?
Heat Pain Pro is a medical device that received FDA 510(k) clearance on 2018-11-09. The listed applicant is Omron Healthcare, Inc.. The 510(k) number is K181992.
When did Heat Pain Pro receive FDA 510(k) clearance?
Heat Pain Pro received FDA 510(k) clearance on 2018-11-09, under 510(k) number K181992.
Who is the listed applicant for Heat Pain Pro?
The FDA 510(k) record lists Omron Healthcare, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Heat Pain Pro?
The FDA product code for Heat Pain Pro is NUH.
其他以 Omron Healthcare, Inc. 為申請人之記錄
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相關器械（代碼：NUH）
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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官方來源
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