Bashir 内血管导管模型7201,Bashir N-X 内血管导管,型号7200
K号: K183290 · 2019-02-25
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器械摘要
常见问题
What is the Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200?
Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200 is a medical device that received FDA 510(k) clearance on 2019-02-25. The listed applicant is Thrombolex, Inc.. The 510(k) number is K183290.
When did Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200 receive FDA 510(k) clearance?
Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200 received FDA 510(k) clearance on 2019-02-25, under 510(k) number K183290.
Who is the listed applicant for Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200?
The FDA 510(k) record lists Thrombolex, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200?
The FDA product code for Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200 is QEY.
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Thrombolex, 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:QEY)
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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