Aesculap PAS-Port 近端吻合术系统
K号: K202124 · 2020-09-02
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器械摘要
Aesculap PAS-Port Proximal Anastomosis System is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2020-09-02 under 510(k) number K202124. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Aesculap PAS-Port Proximal Anastomosis System?
Aesculap PAS-Port Proximal Anastomosis System is a medical device that received FDA 510(k) clearance on 2020-09-02. The listed applicant is Aesculap, Inc.. The 510(k) number is K202124.
When did Aesculap PAS-Port Proximal Anastomosis System receive FDA 510(k) clearance?
Aesculap PAS-Port Proximal Anastomosis System received FDA 510(k) clearance on 2020-09-02, under 510(k) number K202124.
Who is the listed applicant for Aesculap PAS-Port Proximal Anastomosis System?
The FDA 510(k) record lists Aesculap, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Aesculap PAS-Port Proximal Anastomosis System?
The FDA product code for Aesculap PAS-Port Proximal Anastomosis System is FZP.
相关临床试验
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列明Aesculap, 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：FZP）
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。
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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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