KARL STORZ 弹性高清膀胱尿道内窥镜系统
K号: K212476 · 2021-09-03
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器械摘要
常见问题
What is the KARL STORZ Flexible HD Cysto-Urethroscope System?
KARL STORZ Flexible HD Cysto-Urethroscope System is a medical device that received FDA 510(k) clearance on 2021-09-03. The listed applicant is Karl Storz Endoscopy America, Inc.. The 510(k) number is K212476.
When did KARL STORZ Flexible HD Cysto-Urethroscope System receive FDA 510(k) clearance?
KARL STORZ Flexible HD Cysto-Urethroscope System received FDA 510(k) clearance on 2021-09-03, under 510(k) number K212476.
Who is the listed applicant for KARL STORZ Flexible HD Cysto-Urethroscope System?
The FDA 510(k) record lists Karl Storz Endoscopy America, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KARL STORZ Flexible HD Cysto-Urethroscope System?
The FDA product code for KARL STORZ Flexible HD Cysto-Urethroscope System is FAJ.
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Karl Storz Endoscopy America, 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：FAJ）
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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