FDA 510(k)

VOCO回缩膏

K号: K213149 · 2021-12-09

决定日期2021-12-09

产品代码MVL

决定实质等同

器械摘要

VOCO Retraction Paste is the device name listed in this FDA 510(k) record. The listed applicant is Voco GmbH. It received FDA 510(k) clearance on 2021-12-09 under 510(k) number K213149. The device is classified under product code MVL. FDA Decision: Substantially Equivalent.

常见问题

What is the VOCO Retraction Paste?

VOCO Retraction Paste is a medical device that received FDA 510(k) clearance on 2021-12-09. The listed applicant is Voco GmbH. The 510(k) number is K213149.

When did VOCO Retraction Paste receive FDA 510(k) clearance?

VOCO Retraction Paste received FDA 510(k) clearance on 2021-12-09, under 510(k) number K213149.

Who is the listed applicant for VOCO Retraction Paste?

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

What is the FDA product code for VOCO Retraction Paste?

The FDA product code for VOCO Retraction Paste is MVL.

列明Voco GmbH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。

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