RH 非自动化血压计 RH 非自动化血压计配听诊器
K号: K190902 · 2019-05-22
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器械摘要
常见问题
What is the RH non-Automated Blood Pressure Meter RH non-Automated Blood Pressure Meter with Stethoscope?
RH non-Automated Blood Pressure Meter RH non-Automated Blood Pressure Meter with Stethoscope is a medical device that received FDA 510(k) clearance on 2019-05-22. The listed applicant is Wenzhou Renhua Instruments Co., Ltd.. The 510(k) number is K190902.
When did RH non-Automated Blood Pressure Meter RH non-Automated Blood Pressure Meter with Stethoscope receive FDA 510(k) clearance?
RH non-Automated Blood Pressure Meter RH non-Automated Blood Pressure Meter with Stethoscope received FDA 510(k) clearance on 2019-05-22, under 510(k) number K190902.
Who is the listed applicant for RH non-Automated Blood Pressure Meter RH non-Automated Blood Pressure Meter with Stethoscope?
The FDA 510(k) record lists Wenzhou Renhua Instruments Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RH non-Automated Blood Pressure Meter RH non-Automated Blood Pressure Meter with Stethoscope?
The FDA product code for RH non-Automated Blood Pressure Meter RH non-Automated Blood Pressure Meter with Stethoscope is DXQ.
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。
相关器械(代码:DXQ)
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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