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FDA 510(k)

電擊療與電肌肉刺激器(TENS 和 Muscle Stimulator)(JT8012, JT8012B)

K 號:K250053 · 2025-05-09

決定日期2025-05-09
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

TENS AND EMS (TENS and Muscle Stimulator) (JT8012, JT8012B) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Jiantuo Electronics Co., Ltd.. It received FDA 510(k) clearance on 2025-05-09 under 510(k) number K250053. 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 TENS AND EMS (TENS and Muscle Stimulator) (JT8012, JT8012B)?

TENS AND EMS (TENS and Muscle Stimulator) (JT8012, JT8012B) is a medical device that received FDA 510(k) clearance on 2025-05-09. The listed applicant is Shenzhen Jiantuo Electronics Co., Ltd.. The 510(k) number is K250053.

When did TENS AND EMS (TENS and Muscle Stimulator) (JT8012, JT8012B) receive FDA 510(k) clearance?

TENS AND EMS (TENS and Muscle Stimulator) (JT8012, JT8012B) received FDA 510(k) clearance on 2025-05-09, under 510(k) number K250053.

Who is the listed applicant for TENS AND EMS (TENS and Muscle Stimulator) (JT8012, JT8012B)?

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

What is the FDA product code for TENS AND EMS (TENS and Muscle Stimulator) (JT8012, JT8012B)?

The FDA product code for TENS AND EMS (TENS and Muscle Stimulator) (JT8012, JT8012B) is NUH.

相關臨床試驗

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其他以 Shenzhen Jiantuo Electronics Co., Ltd. 為申請人之記錄

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。

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。

官方來源

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