HydroMARK 乳腺活检位点标记
K号: K203097 · 2020-12-16
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器械摘要
常见问题
What is the HydroMARK Breast Biopsy Site Markers?
HydroMARK Breast Biopsy Site Markers is a medical device that received FDA 510(k) clearance on 2020-12-16. The listed applicant is Devicor Medical Products, Inc.. The 510(k) number is K203097.
When did HydroMARK Breast Biopsy Site Markers receive FDA 510(k) clearance?
HydroMARK Breast Biopsy Site Markers received FDA 510(k) clearance on 2020-12-16, under 510(k) number K203097.
Who is the listed applicant for HydroMARK Breast Biopsy Site Markers?
The FDA 510(k) record lists Devicor Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HydroMARK Breast Biopsy Site Markers?
The FDA product code for HydroMARK Breast Biopsy Site Markers is NEU.
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。
列明Devicor Medical Products, Inc.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。
相关器械(代码:NEU)
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。
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