再处理ViewFlex™ Xtra ICE导管
K号: K190478 · 2019-11-14
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器械摘要
常见问题
What is the Reprocessed ViewFlex™ Xtra ICE Catheter?
Reprocessed ViewFlex™ Xtra ICE Catheter is a medical device that received FDA 510(k) clearance on 2019-11-14. The listed applicant is Sterilmed, Inc.. The 510(k) number is K190478.
When did Reprocessed ViewFlex™ Xtra ICE Catheter receive FDA 510(k) clearance?
Reprocessed ViewFlex™ Xtra ICE Catheter received FDA 510(k) clearance on 2019-11-14, under 510(k) number K190478.
Who is the listed applicant for Reprocessed ViewFlex™ Xtra ICE Catheter?
The FDA 510(k) record lists Sterilmed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Reprocessed ViewFlex™ Xtra ICE Catheter?
The FDA product code for Reprocessed ViewFlex™ Xtra ICE Catheter is OWQ.
相关临床试验
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列明Sterilmed, 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:OWQ)
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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