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FDA 510(k)

Nu-beca 過皮電刺激器

K 號：K223151 · 2023-07-19

申請人Nu-Beca & Maxcellent Co.
決定日期2023-07-19
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

Nu-beca Transcutaneous Electrical Nerve Stimulation is the device name listed in this FDA 510(k) record. The listed applicant is Nu-Beca & Maxcellent Co.. It received FDA 510(k) clearance on 2023-07-19 under 510(k) number K223151. 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 Nu-beca Transcutaneous Electrical Nerve Stimulation?

Nu-beca Transcutaneous Electrical Nerve Stimulation is a medical device that received FDA 510(k) clearance on 2023-07-19. The listed applicant is Nu-Beca & Maxcellent Co.. The 510(k) number is K223151.

When did Nu-beca Transcutaneous Electrical Nerve Stimulation receive FDA 510(k) clearance?

Nu-beca Transcutaneous Electrical Nerve Stimulation received FDA 510(k) clearance on 2023-07-19, under 510(k) number K223151.

Who is the listed applicant for Nu-beca Transcutaneous Electrical Nerve Stimulation?

The FDA 510(k) record lists Nu-Beca & Maxcellent Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Nu-beca Transcutaneous Electrical Nerve Stimulation?

The FDA product code for Nu-beca Transcutaneous Electrical Nerve Stimulation is NUH.

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