Separator for therapeutic purposes, membrane automated blood cell/plasma
PMA编号：P820033 · 2026-04-09
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决定日期2026-04-09
PMA 编号P820033
产品代码MDP
设备分类第3类
医疗专科U
咨询委员会GU
请注意，由于您只提供了“GU”这个词，我无法提供完整的翻译。如果您能提供完整的句子或段落，我将能够为您提供准确的翻译。
器械摘要
Separator for therapeutic purposes, membrane automated blood cell/plasma is the device name listed in this FDA 510(k) record. The listed applicant is Asahi Kasei Medical Co., Ltd.. It received FDA 510(k) clearance on 2026-04-09. The device is classified under product code MDP. It was reviewed by the GU advisory panel.
常见问题
What is the Separator for therapeutic purposes, membrane automated blood cell/plasma?
Separator for therapeutic purposes, membrane automated blood cell/plasma is a medical device that received FDA 510(k) clearance on 2026-04-09. The listed applicant is Asahi Kasei Medical Co., Ltd..
When did Separator for therapeutic purposes, membrane automated blood cell/plasma receive FDA 510(k) clearance?
The clearance date for Separator for therapeutic purposes, membrane automated blood cell/plasma can be found in the official FDA records.
谁是用于治疗目的的分离器、膜自动化血细胞/血浆的列名申请人？
The FDA 510(k) record lists Asahi Kasei Medical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
什么是用于治疗目的的分离器，膜自动化血细胞/血浆的FDA产品代码？
FDA用于治疗目的的膜自动血细胞/血浆分离器的产品代码为MDP。
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官方来源
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