Xerosyn
K 號：K233259 · 2024-06-21
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器材摘要
Xerosyn is the device name listed in this FDA 510(k) record. The listed applicant is Xerothera, Inc.. It received FDA 510(k) clearance on 2024-06-21 under 510(k) number K233259. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Xerosyn?
Xerosyn is a medical device that received FDA 510(k) clearance on 2024-06-21. The listed applicant is Xerothera, Inc.. The 510(k) number is K233259.
When did Xerosyn receive FDA 510(k) clearance?
Xerosyn received FDA 510(k) clearance on 2024-06-21, under 510(k) number K233259.
Who is the listed applicant for Xerosyn?
The FDA 510(k) record lists Xerothera, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Xerosyn?
The FDA product code for Xerosyn is MQV.
相關臨床試驗
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相關器械（代碼：MQV）
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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