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FDA 510(k)

加熱TENS/EMS設備,FT-240-1,加熱TENS/EMS設備,FT-240-2

K 號:K221384 · 2022-06-11

決定日期2022-06-11
產品代碼NUH
諮詢委員會NE (請提供完整的英文描述,以便進行翻譯。)
決定相當於

器材摘要

Heating TENS/EMS Device, FT-240-1, Heating TENS/EMS Device, FT-240-2 is the device name listed in this FDA 510(k) record. The listed applicant is Hivox Biotek, Inc.. It received FDA 510(k) clearance on 2022-06-11 under 510(k) number K221384. 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 Heating TENS/EMS Device, FT-240-1, Heating TENS/EMS Device, FT-240-2?

Heating TENS/EMS Device, FT-240-1, Heating TENS/EMS Device, FT-240-2 is a medical device that received FDA 510(k) clearance on 2022-06-11. The listed applicant is Hivox Biotek, Inc.. The 510(k) number is K221384.

When did Heating TENS/EMS Device, FT-240-1, Heating TENS/EMS Device, FT-240-2 receive FDA 510(k) clearance?

Heating TENS/EMS Device, FT-240-1, Heating TENS/EMS Device, FT-240-2 received FDA 510(k) clearance on 2022-06-11, under 510(k) number K221384.

Who is the listed applicant for Heating TENS/EMS Device, FT-240-1, Heating TENS/EMS Device, FT-240-2?

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

What is the FDA product code for Heating TENS/EMS Device, FT-240-1, Heating TENS/EMS Device, FT-240-2?

The FDA product code for Heating TENS/EMS Device, FT-240-1, Heating TENS/EMS Device, FT-240-2 is NUH.

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其他以 Hivox Biotek, Inc. 為申請人之記錄

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相關器械(代碼:NUH)

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官方來源

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