FDA 510(k)

ALTMS 磁刺激治療系統, Blossom TMS 治療系統

K 號：K220625 · 2022-04-06

決定日期2022-04-06

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

ALTMS Magnetic Stimulation Therapy System, Blossom TMS Therapy System is the device name listed in this FDA 510(k) record. The listed applicant is Remed Co., Ltd.. It received FDA 510(k) clearance on 2022-04-06 under 510(k) number K220625. 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 ALTMS Magnetic Stimulation Therapy System, Blossom TMS Therapy System?

ALTMS Magnetic Stimulation Therapy System, Blossom TMS Therapy System is a medical device that received FDA 510(k) clearance on 2022-04-06. The listed applicant is Remed Co., Ltd.. The 510(k) number is K220625.

When did ALTMS Magnetic Stimulation Therapy System, Blossom TMS Therapy System receive FDA 510(k) clearance?

ALTMS Magnetic Stimulation Therapy System, Blossom TMS Therapy System received FDA 510(k) clearance on 2022-04-06, under 510(k) number K220625.

Who is the listed applicant for ALTMS Magnetic Stimulation Therapy System, Blossom TMS Therapy System?

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

What is the FDA product code for ALTMS Magnetic Stimulation Therapy System, Blossom TMS Therapy System?

The FDA product code for ALTMS Magnetic Stimulation Therapy System, Blossom TMS Therapy System is OBP.

其他以 Remed Co., Ltd. 為申請人之記錄

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。

K202537ALTMS 磁刺激治療系統 K202031Talent-Pro 電磁刺激器

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。

K260396KCS rTMS治療系統（經颅磁刺激器）（MetaStim 100，MetaStim 100A）Fidelity BioPharma Co.K260691BTL-699BTL Industries, Inc.K261228QuickVision Ultimate rTMSBrain Ultimate, Inc.K260189馬格韋恩加速經颅磁刺激治療系統（aTMS）Tonica Elektronik A/S K260560Apollo TMS治療系統; Apollo light TMS治療系統Mag & More GmbH K253098Nexstim導向性腦刺激(NBS) 6系統(NBS6)Nexstim Oyj

官方來源

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