Peleton 過濾式單次使用功率系統及配件
K 號：K240071 · 2024-04-04
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器材摘要
Peleton Universal Single Use Power System and Attachments is the device name listed in this FDA 510(k) record. The listed applicant is Peleton Surgical. It received FDA 510(k) clearance on 2024-04-04 under 510(k) number K240071. The device is classified under product code SAM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Peleton Universal Single Use Power System and Attachments?
Peleton Universal Single Use Power System and Attachments is a medical device that received FDA 510(k) clearance on 2024-04-04. The listed applicant is Peleton Surgical. The 510(k) number is K240071.
When did Peleton Universal Single Use Power System and Attachments receive FDA 510(k) clearance?
Peleton Universal Single Use Power System and Attachments received FDA 510(k) clearance on 2024-04-04, under 510(k) number K240071.
Who is the listed applicant for Peleton Universal Single Use Power System and Attachments?
The FDA 510(k) record lists Peleton Surgical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Peleton Universal Single Use Power System and Attachments?
The FDA product code for Peleton Universal Single Use Power System and Attachments is SAM.
相關臨床試驗
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。
官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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