NeuroTrac® MyoPlus Pro (MYO120U)
K 號：K243079 · 2025-06-26
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器材摘要
NeuroTrac® MyoPlus Pro (MYO120U) is the device name listed in this FDA 510(k) record. The listed applicant is Verity Medical , Ltd.. It received FDA 510(k) clearance on 2025-06-26 under 510(k) number K243079. The device is classified under product code KPI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the NeuroTrac® MyoPlus Pro (MYO120U)?
NeuroTrac® MyoPlus Pro (MYO120U) is a medical device that received FDA 510(k) clearance on 2025-06-26. The listed applicant is Verity Medical , Ltd.. The 510(k) number is K243079.
When did NeuroTrac® MyoPlus Pro (MYO120U) receive FDA 510(k) clearance?
NeuroTrac® MyoPlus Pro (MYO120U) received FDA 510(k) clearance on 2025-06-26, under 510(k) number K243079.
Who is the listed applicant for NeuroTrac® MyoPlus Pro (MYO120U)?
The FDA 510(k) record lists Verity Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NeuroTrac® MyoPlus Pro (MYO120U)?
The FDA product code for NeuroTrac® MyoPlus Pro (MYO120U) is KPI.
相關臨床試驗
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相關器械（代碼：KPI）
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。
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官方來源
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