FDA 510(k)

NATRELLE INSPIRA 一次性凝胶植入物测量器

K号: K203229 · 2021-06-02

决定日期2021-06-02

产品代码MRD

决定实质等同

器械摘要

NATRELLE INSPIRA Single Use Sizers for Gel Implants is the device name listed in this FDA 510(k) record. The listed applicant is Allergan. It received FDA 510(k) clearance on 2021-06-02 under 510(k) number K203229. The device is classified under product code MRD. FDA Decision: Substantially Equivalent.

常见问题

What is the NATRELLE INSPIRA Single Use Sizers for Gel Implants?

NATRELLE INSPIRA Single Use Sizers for Gel Implants is a medical device that received FDA 510(k) clearance on 2021-06-02. The listed applicant is Allergan. The 510(k) number is K203229.

When did NATRELLE INSPIRA Single Use Sizers for Gel Implants receive FDA 510(k) clearance?

NATRELLE INSPIRA Single Use Sizers for Gel Implants received FDA 510(k) clearance on 2021-06-02, under 510(k) number K203229.

Who is the listed applicant for NATRELLE INSPIRA Single Use Sizers for Gel Implants?

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

What is the FDA product code for NATRELLE INSPIRA Single Use Sizers for Gel Implants?

The FDA product code for NATRELLE INSPIRA Single Use Sizers for Gel Implants is MRD.

列明Allergan为申报人的其他记录

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