FDA 510(k)

MotiliCap GI监测系统

K号: K250493 · 2025-05-21

决定日期2025-05-21

产品代码NYV

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决定实质等同

器械摘要

MotiliCap GI Monitoring System is the device name listed in this FDA 510(k) record. The listed applicant is Anx Robotica Corporation. It received FDA 510(k) clearance on 2025-05-21 under 510(k) number K250493. The device is classified under product code NYV. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the MotiliCap GI Monitoring System?

MotiliCap GI Monitoring System is a medical device that received FDA 510(k) clearance on 2025-05-21. The listed applicant is Anx Robotica Corporation. The 510(k) number is K250493.

When did MotiliCap GI Monitoring System receive FDA 510(k) clearance?

MotiliCap GI Monitoring System received FDA 510(k) clearance on 2025-05-21, under 510(k) number K250493.

Who is the listed applicant for MotiliCap GI Monitoring System?

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

What is the FDA product code for MotiliCap GI Monitoring System?

The FDA product code for MotiliCap GI Monitoring System is NYV.

列明Anx Robotica 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。

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