FDA 510(k)

NQ TMS用於MDD（NQv1-MU-01）

K 號：K232688 · 2023-12-29

決定日期2023-12-29

產品代碼OBP

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

NQ TMS for MDD (NQv1-MU-01) is the device name listed in this FDA 510(k) record. The listed applicant is Neuroqore, Inc.. It received FDA 510(k) clearance on 2023-12-29 under 510(k) number K232688. The device is classified under product code OBP. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the NQ TMS for MDD (NQv1-MU-01)?

NQ TMS for MDD (NQv1-MU-01) is a medical device that received FDA 510(k) clearance on 2023-12-29. The listed applicant is Neuroqore, Inc.. The 510(k) number is K232688.

When did NQ TMS for MDD (NQv1-MU-01) receive FDA 510(k) clearance?

NQ TMS for MDD (NQv1-MU-01) received FDA 510(k) clearance on 2023-12-29, under 510(k) number K232688.

Who is the listed applicant for NQ TMS for MDD (NQv1-MU-01)?

The FDA 510(k) record lists Neuroqore, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NQ TMS for MDD (NQv1-MU-01)?

The FDA product code for NQ TMS for MDD (NQv1-MU-01) is OBP.

相關器械（代碼：OBP）

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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