FDA 510(k)

3M Curos Tamper-Evident Device, 3M Curos Tamper-Evident Device, Large

K号: K220507 · 2022-05-23

决定日期2022-05-23

产品代码PZW

咨询委员会医疗设备监管文本翻译如下： HO 请注意，由于您没有提供具体的医疗设备监管文本内容，以上仅为示例。请提供具体的文本内容以便进行准确的翻译。

决定实质等同

器械摘要

3M Curos Tamper-Evident Device, 3M Curos Tamper-Evident Device, Large is the device name listed in this FDA 510(k) record. The listed applicant is 3M Company. It received FDA 510(k) clearance on 2022-05-23 under 510(k) number K220507. The device is classified under product code PZW. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the 3M Curos Tamper-Evident Device, 3M Curos Tamper-Evident Device, Large?

3M Curos Tamper-Evident Device, 3M Curos Tamper-Evident Device, Large is a medical device that received FDA 510(k) clearance on 2022-05-23. The listed applicant is 3M Company. The 510(k) number is K220507.

When did 3M Curos Tamper-Evident Device, 3M Curos Tamper-Evident Device, Large receive FDA 510(k) clearance?

3M Curos Tamper-Evident Device, 3M Curos Tamper-Evident Device, Large received FDA 510(k) clearance on 2022-05-23, under 510(k) number K220507.

Who is the listed applicant for 3M Curos Tamper-Evident Device, 3M Curos Tamper-Evident Device, Large?

The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3M Curos Tamper-Evident Device, 3M Curos Tamper-Evident Device, Large?

The FDA product code for 3M Curos Tamper-Evident Device, 3M Curos Tamper-Evident Device, Large is PZW.

列明3M Company为申报人的其他记录

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