KARL STORZ NAV1 Electromagnetic Navigation System
K号: K161555 · 2016-10-21
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器械摘要
常见问题
What is the KARL STORZ NAV1 Electromagnetic Navigation System?
KARL STORZ NAV1 Electromagnetic Navigation System is a medical device that received FDA 510(k) clearance on 2016-10-21. The listed applicant is Karl Storz Endoscopy America, Inc.. The 510(k) number is K161555.
When did KARL STORZ NAV1 Electromagnetic Navigation System receive FDA 510(k) clearance?
KARL STORZ NAV1 Electromagnetic Navigation System received FDA 510(k) clearance on 2016-10-21, under 510(k) number K161555.
Who is the listed applicant for KARL STORZ NAV1 Electromagnetic Navigation 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 NAV1 Electromagnetic Navigation System?
The FDA product code for KARL STORZ NAV1 Electromagnetic Navigation System is PGW.
相关临床试验
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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：PGW）
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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