NEXA 負壓創傷治療系統
K 號：K162610 · 2017-06-08
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器材摘要
NEXA Negative Pressure Wound Therapy System is the device name listed in this FDA 510(k) record. The listed applicant is Nexa Medical , Ltd.. It received FDA 510(k) clearance on 2017-06-08 under 510(k) number K162610. The device is classified under product code OMP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the NEXA Negative Pressure Wound Therapy System?
NEXA Negative Pressure Wound Therapy System is a medical device that received FDA 510(k) clearance on 2017-06-08. The listed applicant is Nexa Medical , Ltd.. The 510(k) number is K162610.
When did NEXA Negative Pressure Wound Therapy System receive FDA 510(k) clearance?
NEXA Negative Pressure Wound Therapy System received FDA 510(k) clearance on 2017-06-08, under 510(k) number K162610.
Who is the listed applicant for NEXA Negative Pressure Wound Therapy System?
The FDA 510(k) record lists Nexa Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NEXA Negative Pressure Wound Therapy System?
The FDA product code for NEXA Negative Pressure Wound Therapy System is OMP.
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相關器械（代碼：OMP）
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
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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