FDA 510(k)

BenQ 诊断超声系统

K号: K181313 · 2018-08-27

决定日期2018-08-27

产品代码IYN

咨询委员会RA

决定实质等同

器械摘要

BenQ Diagnostic Ultrasound System is the device name listed in this FDA 510(k) record. The listed applicant is Qisda Corporation. It received FDA 510(k) clearance on 2018-08-27 under 510(k) number K181313. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the BenQ Diagnostic Ultrasound System?

BenQ Diagnostic Ultrasound System is a medical device that received FDA 510(k) clearance on 2018-08-27. The listed applicant is Qisda Corporation. The 510(k) number is K181313.

When did BenQ Diagnostic Ultrasound System receive FDA 510(k) clearance?

BenQ Diagnostic Ultrasound System received FDA 510(k) clearance on 2018-08-27, under 510(k) number K181313.

Who is the listed applicant for BenQ Diagnostic Ultrasound System?

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

What is the FDA product code for BenQ Diagnostic Ultrasound System?

The FDA product code for BenQ Diagnostic Ultrasound System is IYN.

列明Qisda 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。

K192254InnoSight 诊断超声系统 K172056InnoSight 诊断超声系统

相关器械（代码：IYN）

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。

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。