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FDA 510(k)

BD Phoenix自動微生物學系統-Ertapenem 0.0625-8 mcg/ml

K 號:K151320 · 2016-01-15

決定日期2016-01-15
產品代碼LON
諮詢委員會MI (請提供完整的描述文本,以便進行翻譯。)
決定相當於

器材摘要

BD Phoenix Automated Microbiology System-Ertapenem 0.0625-8 mcg/ml is the device name listed in this FDA 510(k) record. The listed applicant is Becton, Dickinson and Company. It received FDA 510(k) clearance on 2016-01-15 under 510(k) number K151320. The device is classified under product code LON. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the BD Phoenix Automated Microbiology System-Ertapenem 0.0625-8 mcg/ml?

BD Phoenix Automated Microbiology System-Ertapenem 0.0625-8 mcg/ml is a medical device that received FDA 510(k) clearance on 2016-01-15. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K151320.

When did BD Phoenix Automated Microbiology System-Ertapenem 0.0625-8 mcg/ml receive FDA 510(k) clearance?

BD Phoenix Automated Microbiology System-Ertapenem 0.0625-8 mcg/ml received FDA 510(k) clearance on 2016-01-15, under 510(k) number K151320.

Who is the listed applicant for BD Phoenix Automated Microbiology System-Ertapenem 0.0625-8 mcg/ml?

The FDA 510(k) record lists Becton, Dickinson and Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BD Phoenix Automated Microbiology System-Ertapenem 0.0625-8 mcg/ml?

The FDA product code for BD Phoenix Automated Microbiology System-Ertapenem 0.0625-8 mcg/ml is LON.

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其他以 Becton, Dickinson and Company 為申請人之記錄

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相關器械(代碼:LON)

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