FDA 510(k)

MECTA Sigma

K号: K192834 · 2020-04-26

决定日期2020-04-26

产品代码QGH

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决定实质等同

器械摘要

MECTA Sigma is the device name listed in this FDA 510(k) record. The listed applicant is Mecta Corporation. It received FDA 510(k) clearance on 2020-04-26 under 510(k) number K192834. The device is classified under product code QGH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the MECTA Sigma?

MECTA Sigma is a medical device that received FDA 510(k) clearance on 2020-04-26. The listed applicant is Mecta Corporation. The 510(k) number is K192834.

When did MECTA Sigma receive FDA 510(k) clearance?

MECTA Sigma received FDA 510(k) clearance on 2020-04-26, under 510(k) number K192834.

Who is the listed applicant for MECTA Sigma?

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

What is the FDA product code for MECTA Sigma?

The FDA product code for MECTA Sigma is QGH.

列明Mecta 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。

K201309ECT棉咬合块-大号，ECT棉咬合块-中号

官方来源

在 FDA 数据库中查看 →

数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。

器械摘要

常见问题

相关临床试验

列明Mecta Corporation为申报人的其他记录

官方来源