Quiver 吸引泵
K号: K232831 · 2024-02-22
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决定日期2024-02-22
产品代码BTA
咨询委员会SU
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决定实质等同
器械摘要
Quiver Aspiration Pump is the device name listed in this FDA 510(k) record. The listed applicant is Anoxia Medical, Inc.. It received FDA 510(k) clearance on 2024-02-22 under 510(k) number K232831. The device is classified under product code BTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Quiver Aspiration Pump?
Quiver Aspiration Pump is a medical device that received FDA 510(k) clearance on 2024-02-22. The listed applicant is Anoxia Medical, Inc.. The 510(k) number is K232831.
When did Quiver Aspiration Pump receive FDA 510(k) clearance?
Quiver Aspiration Pump received FDA 510(k) clearance on 2024-02-22, under 510(k) number K232831.
Who is the listed applicant for Quiver Aspiration Pump?
The FDA 510(k) record lists Anoxia Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Quiver Aspiration Pump?
The FDA product code for Quiver Aspiration Pump is BTA.
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Anoxia Medical, 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：BTA）
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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