FDA 510(k)

SunStim Peripheral Nerve Stimulator/Sunstim Plus Peripheral Nerve Stimulator

K番号: K153045 · 2016-05-13

決定日2016-05-13

製品コードBXN

諮問委員会AN 当社の医療機器は、FDA（米国食品医薬品局）の規制に従って製造・販売されています。製品は、510(k)通知書およびPMA（プレマーケティング評価）を通じて承認を受けています。臨床試験情報は、NCT（臨床試験登録番号）およびPMID（PubMed ID）で確認できます。詳細情報や製品の詳細については、以下のURLをご参照ください。 [URL]

決定Substantially Equivalent

医療機器の概要

SunStim Peripheral Nerve Stimulator/Sunstim Plus Peripheral Nerve Stimulator is the device name listed in this FDA 510(k) record. The listed applicant is Easy Med Instrument Co., Ltd.. It received FDA 510(k) clearance on 2016-05-13 under 510(k) number K153045. The device is classified under product code BXN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the SunStim Peripheral Nerve Stimulator/Sunstim Plus Peripheral Nerve Stimulator?

SunStim Peripheral Nerve Stimulator/Sunstim Plus Peripheral Nerve Stimulator is a medical device that received FDA 510(k) clearance on 2016-05-13. The listed applicant is Easy Med Instrument Co., Ltd.. The 510(k) number is K153045.

When did SunStim Peripheral Nerve Stimulator/Sunstim Plus Peripheral Nerve Stimulator receive FDA 510(k) clearance?

SunStim Peripheral Nerve Stimulator/Sunstim Plus Peripheral Nerve Stimulator received FDA 510(k) clearance on 2016-05-13, under 510(k) number K153045.

Who is the listed applicant for SunStim Peripheral Nerve Stimulator/Sunstim Plus Peripheral Nerve Stimulator?

The FDA 510(k) record lists Easy Med Instrument Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SunStim Peripheral Nerve Stimulator/Sunstim Plus Peripheral Nerve Stimulator?

The FDA product code for SunStim Peripheral Nerve Stimulator/Sunstim Plus Peripheral Nerve Stimulator is BXN.

公式ソース

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SunStim Peripheral Nerve Stimulator/Sunstim Plus Peripheral Nerve Stimulator

医療機器の概要

よくある質問

関連する臨床試験

関連機器（コード：BXN）

公式ソース