FDA 510(k)

Novidia 通用粘合剂

K号: K183391 · 2019-09-24

决定日期2019-09-24

产品代码KLE

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决定实质等同

器械摘要

Novidia Universal Bond is the device name listed in this FDA 510(k) record. The listed applicant is Nobio , Ltd.. It received FDA 510(k) clearance on 2019-09-24 under 510(k) number K183391. The device is classified under product code KLE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Novidia Universal Bond?

Novidia Universal Bond is a medical device that received FDA 510(k) clearance on 2019-09-24. The listed applicant is Nobio , Ltd.. The 510(k) number is K183391.

When did Novidia Universal Bond receive FDA 510(k) clearance?

Novidia Universal Bond received FDA 510(k) clearance on 2019-09-24, under 510(k) number K183391.

Who is the listed applicant for Novidia Universal Bond?

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

What is the FDA product code for Novidia Universal Bond?

The FDA product code for Novidia Universal Bond is KLE.

列明Nobio , Ltd.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。

K201010Infinix Universal Composite, Infinix Flowable Composite, Infinix Bulk Fill Flow Composite K182921Infinix Universal Composite K182714Novidia 大量填充流动复合体 K182580Novidia 流动复合体

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