膠粘劑，硬膜
PMA 核准號：P220014 · 2026-08-05
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器材摘要
Sealant, dural is the device name listed in this FDA 510(k) record. The listed applicant is Pramand, LLC. It received FDA 510(k) clearance on 2026-08-05. The device is classified under product code NQR. It was reviewed by the NE advisory panel.
常見問題
What is the Sealant, dural?
Sealant, dural is a medical device that received FDA 510(k) clearance on 2026-08-05. The listed applicant is Pramand, LLC.
When did Sealant, dural receive FDA 510(k) clearance?
The clearance date for Sealant, dural can be found in the official FDA records.
誰是Sealant, dural的登記申請人？
The FDA 510(k) record lists Pramand, LLC as the applicant. This does not by itself establish the device manufacturer.
FDA產品代碼是什麼？Sealant, dural？
FDA產品代碼，對於膠粘劑、硬膜類產品為NQR。
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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