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FDA 510(k)

SP NEWTRON CAN-A；MODULE NEWTRON CAN-A EMB；SUPPORT XINETIC；NWT CAN SLIM LED CORD G3 短；NWT CAN SLIM LED CORD G3 長

K 號：K233922 · 2024-03-11

申請人Satelec - Acteon Group
決定日期2024-03-11
產品代碼ELC
諮詢委員會DE
決定相當於

器材摘要

SP NEWTRON CAN-A; MODULE NEWTRON CAN-A EMB; SUPPORT XINETIC; NWT CAN SLIM LED CORD G3 SHORT; NWT CAN SLIM LED CORD G3 LONG is the device name listed in this FDA 510(k) record. The listed applicant is Satelec - Acteon Group. It received FDA 510(k) clearance on 2024-03-11 under 510(k) number K233922. The device is classified under product code ELC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the SP NEWTRON CAN-A; MODULE NEWTRON CAN-A EMB; SUPPORT XINETIC; NWT CAN SLIM LED CORD G3 SHORT; NWT CAN SLIM LED CORD G3 LONG?

SP NEWTRON CAN-A; MODULE NEWTRON CAN-A EMB; SUPPORT XINETIC; NWT CAN SLIM LED CORD G3 SHORT; NWT CAN SLIM LED CORD G3 LONG is a medical device that received FDA 510(k) clearance on 2024-03-11. The listed applicant is Satelec - Acteon Group. The 510(k) number is K233922.

When did SP NEWTRON CAN-A; MODULE NEWTRON CAN-A EMB; SUPPORT XINETIC; NWT CAN SLIM LED CORD G3 SHORT; NWT CAN SLIM LED CORD G3 LONG receive FDA 510(k) clearance?

SP NEWTRON CAN-A; MODULE NEWTRON CAN-A EMB; SUPPORT XINETIC; NWT CAN SLIM LED CORD G3 SHORT; NWT CAN SLIM LED CORD G3 LONG received FDA 510(k) clearance on 2024-03-11, under 510(k) number K233922.

Who is the listed applicant for SP NEWTRON CAN-A; MODULE NEWTRON CAN-A EMB; SUPPORT XINETIC; NWT CAN SLIM LED CORD G3 SHORT; NWT CAN SLIM LED CORD G3 LONG?

The FDA 510(k) record lists Satelec - Acteon Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SP NEWTRON CAN-A; MODULE NEWTRON CAN-A EMB; SUPPORT XINETIC; NWT CAN SLIM LED CORD G3 SHORT; NWT CAN SLIM LED CORD G3 LONG?

The FDA product code for SP NEWTRON CAN-A; MODULE NEWTRON CAN-A EMB; SUPPORT XINETIC; NWT CAN SLIM LED CORD G3 SHORT; NWT CAN SLIM LED CORD G3 LONG is ELC.

相關臨床試驗

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其他以 Satelec - Acteon Group 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。

K172137PIEZOTOME CUBE

相關器械（代碼：ELC）

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官方來源

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