REGER 雾化噴霧灌流針管
K 號：K231622 · 2023-09-29
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器材摘要
REGER Nebulizer Irrigation Cannula is the device name listed in this FDA 510(k) record. The listed applicant is Reger Medizintechnik, GmbH. It received FDA 510(k) clearance on 2023-09-29 under 510(k) number K231622. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the REGER Nebulizer Irrigation Cannula?
REGER Nebulizer Irrigation Cannula is a medical device that received FDA 510(k) clearance on 2023-09-29. The listed applicant is Reger Medizintechnik, GmbH. The 510(k) number is K231622.
When did REGER Nebulizer Irrigation Cannula receive FDA 510(k) clearance?
REGER Nebulizer Irrigation Cannula received FDA 510(k) clearance on 2023-09-29, under 510(k) number K231622.
Who is the listed applicant for REGER Nebulizer Irrigation Cannula?
The FDA 510(k) record lists Reger Medizintechnik, GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for REGER Nebulizer Irrigation Cannula?
The FDA product code for REGER Nebulizer Irrigation Cannula is GCJ.
相關臨床試驗
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相關器械（代碼：GCJ）
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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