MD-6000S Bladder Scanner
K 號：K260313 · 2026-09-24
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器材摘要
MD-6000S Bladder Scanner is the device name listed in this FDA 510(k) record. The listed applicant is MEDA Co., Ltd.. It received FDA 510(k) clearance on 2026-09-24 under 510(k) number K260313. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the MD-6000S Bladder Scanner?
MD-6000S Bladder Scanner is a medical device that received FDA 510(k) clearance on 2026-09-24. The listed applicant is MEDA Co., Ltd.. The 510(k) number is K260313.
When did MD-6000S Bladder Scanner receive FDA 510(k) clearance?
MD-6000S Bladder Scanner received FDA 510(k) clearance on 2026-09-24, under 510(k) number K260313.
Who is the listed applicant for MD-6000S Bladder Scanner?
The FDA 510(k) record lists MEDA Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MD-6000S Bladder Scanner?
The FDA product code for MD-6000S Bladder Scanner is IYO.
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其他以 MEDA Co., Ltd. 為申請人之記錄
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相關器械（代碼：IYO）
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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