Nulife
K 號：K210969 · 2021-11-03
廣告
器材摘要
Nulife is the device name listed in this FDA 510(k) record. The listed applicant is Mrk Healthcare Pvt, Ltd.. It received FDA 510(k) clearance on 2021-11-03 under 510(k) number K210969. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Nulife?
Nulife is a medical device that received FDA 510(k) clearance on 2021-11-03. The listed applicant is Mrk Healthcare Pvt, Ltd.. The 510(k) number is K210969.
When did Nulife receive FDA 510(k) clearance?
Nulife received FDA 510(k) clearance on 2021-11-03, under 510(k) number K210969.
Who is the listed applicant for Nulife?
The FDA 510(k) record lists Mrk Healthcare Pvt, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Nulife?
The FDA product code for Nulife is KGO.
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。
相關器械（代碼：KGO）
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。
K260558乳膠無粉外科手術手套，已經通過與化學治療藥物及芬太尼鹽酸鹽的合用測試；含膠狀燕麥粉的乳膠無粉外科手術手套，已經通過與化學治療藥物及芬太尼鹽酸鹽的合用測試Hartalega NGC Sdn. Bhd.K253060無菌乳膠無粉外科手套Protect Gloves Company LimitedK250313無菌粉末釋放合成橡膠外科醫用手套，綠色，已測試與化療藥物及胃酸使用相容Harps Europe Manufacturing GmbHK240790多異戊二烯外科手套Suzhou Colour-Way New Material Co., Ltd.K232079天然橡膠乳膠外科手套，無粉，无菌，已測試與化療藥物及芬太尼（綠色）相容；天然橡膠乳膠（去膜&塗層）/（去膜&包裝）外科手套，無粉，无菌，已測試與化療藥物及芬太尼相容Wrp Asia Pacific Sdn. Bhd.K232444無菌無粉乳膠外科手套，已檢驗適合與化療藥物使用Grand Work Plastic Products Co., Ltd.
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。
廣告