Exsalta
K号: K221676 · 2022-09-16
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器械摘要
Exsalta is the device name listed in this FDA 510(k) record. The listed applicant is Drw Medical. It received FDA 510(k) clearance on 2022-09-16 under 510(k) number K221676. 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 Exsalta?
Exsalta is a medical device that received FDA 510(k) clearance on 2022-09-16. The listed applicant is Drw Medical. The 510(k) number is K221676.
When did Exsalta receive FDA 510(k) clearance?
Exsalta received FDA 510(k) clearance on 2022-09-16, under 510(k) number K221676.
Who is the listed applicant for Exsalta?
The FDA 510(k) record lists Drw Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Exsalta?
The FDA product code for Exsalta is BTA.
相关临床试验
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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
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