FDA 510(k)

MR Q；MR Q 仰卧；MR Q SLT

K号: K232417 · 2024-01-25

决定日期2024-01-25

产品代码HQF

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决定实质等同

器械摘要

MR Q; MR Q SUPINE; MR Q SLT is the device name listed in this FDA 510(k) record. The listed applicant is Meridian AG. It received FDA 510(k) clearance on 2024-01-25 under 510(k) number K232417. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the MR Q; MR Q SUPINE; MR Q SLT?

MR Q; MR Q SUPINE; MR Q SLT is a medical device that received FDA 510(k) clearance on 2024-01-25. The listed applicant is Meridian AG. The 510(k) number is K232417.

When did MR Q; MR Q SUPINE; MR Q SLT receive FDA 510(k) clearance?

MR Q; MR Q SUPINE; MR Q SLT received FDA 510(k) clearance on 2024-01-25, under 510(k) number K232417.

Who is the listed applicant for MR Q; MR Q SUPINE; MR Q SLT?

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

What is the FDA product code for MR Q; MR Q SUPINE; MR Q SLT?

The FDA product code for MR Q; MR Q SUPINE; MR Q SLT is HQF.

列明Meridian AG为申报人的其他记录

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。

K231011Merilas 532短脉冲，Merilas 577短脉冲，Merilas 810短脉冲 K160677MICRORUPTOR 6

官方来源

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