FDA 510(k)

肌肉刺激器

K 號：K231648 · 2024-03-01

決定日期2024-03-01

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

Muscle Stimulator is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Yiran Intelligent Co., Ltd.. It received FDA 510(k) clearance on 2024-03-01 under 510(k) number K231648. 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 Muscle Stimulator?

Muscle Stimulator is a medical device that received FDA 510(k) clearance on 2024-03-01. The listed applicant is Shenzhen Yiran Intelligent Co., Ltd.. The 510(k) number is K231648.

When did Muscle Stimulator receive FDA 510(k) clearance?

Muscle Stimulator received FDA 510(k) clearance on 2024-03-01, under 510(k) number K231648.

Who is the listed applicant for Muscle Stimulator?

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

What is the FDA product code for Muscle Stimulator?

The FDA product code for Muscle Stimulator is NUH.

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。

K261131電動肌肉刺激器（AST-105DJ、AST-105EJ、AST-105BJ、AST-105GJ、AST-303J、AST-309J、AST-310J；AST-300Q、AST-300Q-A、AST-500B；AST-500G、AST-500F；AST-500N；AST-500C、AST-500K、AST-500A；AST-300E、AST-500M、AST-500U、AST-500D；AST-500E。）Shenzhen Osto Medical Technology Co.,Ltd K260412TENS 7000 可充電 4 頻道 (TENS 7000H)Shenzhen Dongdixin Technology Co., Ltd.K260425TENS / EMS 裝置（FT-247 系列產品）（FT-247，FT-237）Hivox Biotek, Inc.K253896TENS/EMS 裝置（GUSE01）Globalcare Medical Technology Co., Ltd.K253305電擊療與電肌肉刺激器（TENS 和 Muscle Stimulator）(JT1065, JT1080, JT2080, JT9034)Shenzhen Jiantuo Electronics Co., Ltd.K253740TENS&EMS (HZ9151B, HZ9151C, HZ9151D)Hong Qiangxing (Shenzhen) Electronics Limited

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