FDA 510(k)

Myriad SPECTRA 光源

K号: K232567 · 2024-03-14

决定日期2024-03-14

产品代码QFX

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决定实质等同

器械摘要

Myriad SPECTRA Light Source is the device name listed in this FDA 510(k) record. The listed applicant is Nico Corporation. It received FDA 510(k) clearance on 2024-03-14 under 510(k) number K232567. The device is classified under product code QFX. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Myriad SPECTRA Light Source?

Myriad SPECTRA Light Source is a medical device that received FDA 510(k) clearance on 2024-03-14. The listed applicant is Nico Corporation. The 510(k) number is K232567.

When did Myriad SPECTRA Light Source receive FDA 510(k) clearance?

Myriad SPECTRA Light Source received FDA 510(k) clearance on 2024-03-14, under 510(k) number K232567.

Who is the listed applicant for Myriad SPECTRA Light Source?

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

What is the FDA product code for Myriad SPECTRA Light Source?

The FDA product code for Myriad SPECTRA Light Source is QFX.

列明Nico Corporation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。

K191599NICO Myriad NOVUS K182340NICO Myriad K172433NICO BrainPath K161307NICO Myriad K162075NICO TRIOwand

官方来源

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