免责声明: 本站汇总 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公开数据,仅供一般参考,不构成医疗建议、诊断、治疗建议或投资建议。

FDA 510(k)

BioTracker 2.0

K号: K253306 · 2026-06-26

决定日期2026-06-26
产品代码
决定实质等同

器械摘要

BioTracker 2.0 is the device name listed in this FDA 510(k) record. The listed applicant is Biotracker, LLC. It received FDA 510(k) clearance on 2026-06-26 under 510(k) number K253306. FDA Decision: Substantially Equivalent.

常见问题

What is the BioTracker 2.0?

BioTracker 2.0 is a medical device that received FDA 510(k) clearance on 2026-06-26. The listed applicant is Biotracker, LLC. The 510(k) number is K253306.

When did BioTracker 2.0 receive FDA 510(k) clearance?

BioTracker 2.0 received FDA 510(k) clearance on 2026-06-26, under 510(k) number K253306.

Who is the listed applicant for BioTracker 2.0?

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

相关临床试验

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。

↑