EvaQMax烟雾排放系统
K号: K192035 · 2019-08-29
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器械摘要
EvaQMax Smoke Evacuation System is the device name listed in this FDA 510(k) record. The listed applicant is Bio Protech, Inc.. It received FDA 510(k) clearance on 2019-08-29 under 510(k) number K192035. The device is classified under product code FYD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the EvaQMax Smoke Evacuation System?
EvaQMax Smoke Evacuation System is a medical device that received FDA 510(k) clearance on 2019-08-29. The listed applicant is Bio Protech, Inc.. The 510(k) number is K192035.
When did EvaQMax Smoke Evacuation System receive FDA 510(k) clearance?
EvaQMax Smoke Evacuation System received FDA 510(k) clearance on 2019-08-29, under 510(k) number K192035.
Who is the listed applicant for EvaQMax Smoke Evacuation System?
The FDA 510(k) record lists Bio Protech, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EvaQMax Smoke Evacuation System?
The FDA product code for EvaQMax Smoke Evacuation System is FYD.
相关临床试验
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列明Bio Protech, 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：FYD）
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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