Alma TED+ 系統
K 號：K251684 · 2026-06-05
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器材摘要
Alma TED+ System is the device name listed in this FDA 510(k) record. The listed applicant is Alma Lasers, Inc.. It received FDA 510(k) clearance on 2026-06-05 under 510(k) number K251684. The device is classified under product code OAP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Alma TED+ System?
Alma TED+ System is a medical device that received FDA 510(k) clearance on 2026-06-05. The listed applicant is Alma Lasers, Inc.. The 510(k) number is K251684.
When did Alma TED+ System receive FDA 510(k) clearance?
Alma TED+ System received FDA 510(k) clearance on 2026-06-05, under 510(k) number K251684.
Who is the listed applicant for Alma TED+ System?
The FDA 510(k) record lists Alma Lasers, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Alma TED+ System?
The FDA product code for Alma TED+ System is OAP.
相關臨床試驗
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其他以 Alma Lasers, Inc. 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。
相關器械（代碼：OAP）
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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