電擊療電極
K 號：K160081 · 2016-10-19
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器材摘要
TENS Electrodes is the device name listed in this FDA 510(k) record. The listed applicant is Cathay Manufacturing Corp.. It received FDA 510(k) clearance on 2016-10-19 under 510(k) number K160081. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the TENS Electrodes?
TENS Electrodes is a medical device that received FDA 510(k) clearance on 2016-10-19. The listed applicant is Cathay Manufacturing Corp.. The 510(k) number is K160081.
When did TENS Electrodes receive FDA 510(k) clearance?
TENS Electrodes received FDA 510(k) clearance on 2016-10-19, under 510(k) number K160081.
Who is the listed applicant for TENS Electrodes?
The FDA 510(k) record lists Cathay Manufacturing Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TENS Electrodes?
The FDA product code for TENS Electrodes is GXY.
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相關器械（代碼：GXY）
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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