FDA 510(k)

Fehling-Punches

K号: K153243 · 2016-08-04

决定日期2016-08-04

产品代码HAE

咨询委员会NE 请注意，您提供的文本“NE”不足以进行翻译，因为它不是一个完整的句子或描述。请提供完整的医疗设备监管文本，以便我能够进行准确的翻译。

决定实质等同

器械摘要

Fehling-Punches is the device name listed in this FDA 510(k) record. The listed applicant is Fehling Instruments GmbH & Co. KG. It received FDA 510(k) clearance on 2016-08-04 under 510(k) number K153243. The device is classified under product code HAE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Fehling-Punches?

Fehling-Punches is a medical device that received FDA 510(k) clearance on 2016-08-04. The listed applicant is Fehling Instruments GmbH & Co. KG. The 510(k) number is K153243.

When did Fehling-Punches receive FDA 510(k) clearance?

Fehling-Punches received FDA 510(k) clearance on 2016-08-04, under 510(k) number K153243.

Who is the listed applicant for Fehling-Punches?

The FDA 510(k) record lists Fehling Instruments GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Fehling-Punches?

The FDA product code for Fehling-Punches is HAE.

列明Fehling Instruments GmbH & Co. KG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。

K170726Biopsy Forceps

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。