UC-1800 自动尿液分析仪，URIT 11FA 尿试纸条，URIT 12FA 尿试纸条
K号: K232317 · 2024-04-26
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器械摘要
常见问题
What is the UC-1800 Automatic Urine Analyzer, URIT 11FA Urine Reagent Strips, URIT 12FA Urine Reagent Strips?
UC-1800 Automatic Urine Analyzer, URIT 11FA Urine Reagent Strips, URIT 12FA Urine Reagent Strips is a medical device that received FDA 510(k) clearance on 2024-04-26. The listed applicant is Urit Medical Electronic Co., Ltd.. The 510(k) number is K232317.
When did UC-1800 Automatic Urine Analyzer, URIT 11FA Urine Reagent Strips, URIT 12FA Urine Reagent Strips receive FDA 510(k) clearance?
UC-1800 Automatic Urine Analyzer, URIT 11FA Urine Reagent Strips, URIT 12FA Urine Reagent Strips received FDA 510(k) clearance on 2024-04-26, under 510(k) number K232317.
Who is the listed applicant for UC-1800 Automatic Urine Analyzer, URIT 11FA Urine Reagent Strips, URIT 12FA Urine Reagent Strips?
The FDA 510(k) record lists Urit Medical Electronic Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UC-1800 Automatic Urine Analyzer, URIT 11FA Urine Reagent Strips, URIT 12FA Urine Reagent Strips?
The FDA product code for UC-1800 Automatic Urine Analyzer, URIT 11FA Urine Reagent Strips, URIT 12FA Urine Reagent Strips is JIO.
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官方来源
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