1.5T 腹腔内线圈，3.0T 腹腔内线圈，ER 线圈支架
K号: K191539 · 2020-01-31
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器械摘要
常见问题
What is the 1.5T Endorectal Coil, 3.0T Endorectal Coil, ER Coil Support?
1.5T Endorectal Coil, 3.0T Endorectal Coil, ER Coil Support is a medical device that received FDA 510(k) clearance on 2020-01-31. The listed applicant is Rapid Biomedical GmbH. The 510(k) number is K191539.
When did 1.5T Endorectal Coil, 3.0T Endorectal Coil, ER Coil Support receive FDA 510(k) clearance?
1.5T Endorectal Coil, 3.0T Endorectal Coil, ER Coil Support received FDA 510(k) clearance on 2020-01-31, under 510(k) number K191539.
Who is the listed applicant for 1.5T Endorectal Coil, 3.0T Endorectal Coil, ER Coil Support?
The FDA 510(k) record lists Rapid Biomedical GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 1.5T Endorectal Coil, 3.0T Endorectal Coil, ER Coil Support?
The FDA product code for 1.5T Endorectal Coil, 3.0T Endorectal Coil, ER Coil Support is MOS.
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Rapid Biomedical GmbH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：MOS）
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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