FDA 510(k)

Trak Plus 男性生育能力检测系统

K号: K172514 · 2017-11-17

决定日期2017-11-17

产品代码POV

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决定实质等同

器械摘要

Trak Plus Male Fertility Testing System is the device name listed in this FDA 510(k) record. The listed applicant is Sandstone Diagnostics, Inc.. It received FDA 510(k) clearance on 2017-11-17 under 510(k) number K172514. The device is classified under product code POV. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Trak Plus Male Fertility Testing System?

Trak Plus Male Fertility Testing System is a medical device that received FDA 510(k) clearance on 2017-11-17. The listed applicant is Sandstone Diagnostics, Inc.. The 510(k) number is K172514.

When did Trak Plus Male Fertility Testing System receive FDA 510(k) clearance?

Trak Plus Male Fertility Testing System received FDA 510(k) clearance on 2017-11-17, under 510(k) number K172514.

Who is the listed applicant for Trak Plus Male Fertility Testing System?

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

What is the FDA product code for Trak Plus Male Fertility Testing System?

The FDA product code for Trak Plus Male Fertility Testing System is POV.

列明Sandstone Diagnostics, Inc.为申报人的其他记录

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K153683Trak男性生育力检测系统

官方来源

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