Apyx 氦等离子体发生器 (APYX-200H/P, APYX-JS3/RS3)
K号: K192867 · 2019-10-31
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器械摘要
常见问题
What is the Apyx Helium Plasma Generator (APYX-200H/P, APYX-JS3/RS3)?
Apyx Helium Plasma Generator (APYX-200H/P, APYX-JS3/RS3) is a medical device that received FDA 510(k) clearance on 2019-10-31. The listed applicant is Bovie Medical Corporation Dba Apyx Medical Corporation. The 510(k) number is K192867.
When did Apyx Helium Plasma Generator (APYX-200H/P, APYX-JS3/RS3) receive FDA 510(k) clearance?
Apyx Helium Plasma Generator (APYX-200H/P, APYX-JS3/RS3) received FDA 510(k) clearance on 2019-10-31, under 510(k) number K192867.
Who is the listed applicant for Apyx Helium Plasma Generator (APYX-200H/P, APYX-JS3/RS3)?
The FDA 510(k) record lists Bovie Medical Corporation Dba Apyx Medical Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Apyx Helium Plasma Generator (APYX-200H/P, APYX-JS3/RS3)?
The FDA product code for Apyx Helium Plasma Generator (APYX-200H/P, APYX-JS3/RS3) is GEI.
相关临床试验
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列明Bovie Medical Corporation Dba Apyx Medical Corporation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:GEI)
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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