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FDA 510(k)

Ranfac 侧入路骨髓抽吸针 (CRVS-BMA-LA)

K号: K223612 · 2023-02-21

决定日期2023-02-21
产品代码KNW
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。
决定实质等同

器械摘要

Ranfac Lateral Access Bone Marrow Aspiration Needle (CRVS-BMA-LA) is the device name listed in this FDA 510(k) record. The listed applicant is Ranfac Corporation. It received FDA 510(k) clearance on 2023-02-21 under 510(k) number K223612. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Ranfac Lateral Access Bone Marrow Aspiration Needle (CRVS-BMA-LA)?

Ranfac Lateral Access Bone Marrow Aspiration Needle (CRVS-BMA-LA) is a medical device that received FDA 510(k) clearance on 2023-02-21. The listed applicant is Ranfac Corporation. The 510(k) number is K223612.

When did Ranfac Lateral Access Bone Marrow Aspiration Needle (CRVS-BMA-LA) receive FDA 510(k) clearance?

Ranfac Lateral Access Bone Marrow Aspiration Needle (CRVS-BMA-LA) received FDA 510(k) clearance on 2023-02-21, under 510(k) number K223612.

Who is the listed applicant for Ranfac Lateral Access Bone Marrow Aspiration Needle (CRVS-BMA-LA)?

The FDA 510(k) record lists Ranfac Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Ranfac Lateral Access Bone Marrow Aspiration Needle (CRVS-BMA-LA)?

The FDA product code for Ranfac Lateral Access Bone Marrow Aspiration Needle (CRVS-BMA-LA) is KNW.

相关临床试验

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列明Ranfac Corporation为申报人的其他记录

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相关器械(代码:KNW)

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。

官方来源

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