STERRAD NX 配备 ALLClear 技术
K号: K220404 · 2022-05-16
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器械摘要
常见问题
What is the STERRAD NX with ALLClear Technology?
STERRAD NX with ALLClear Technology is a medical device that received FDA 510(k) clearance on 2022-05-16. The listed applicant is Advanced Sterilization Products, Inc.. The 510(k) number is K220404.
When did STERRAD NX with ALLClear Technology receive FDA 510(k) clearance?
STERRAD NX with ALLClear Technology received FDA 510(k) clearance on 2022-05-16, under 510(k) number K220404.
Who is the listed applicant for STERRAD NX with ALLClear Technology?
The FDA 510(k) record lists Advanced Sterilization Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STERRAD NX with ALLClear Technology?
The FDA product code for STERRAD NX with ALLClear Technology is MLR.
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Advanced Sterilization Products, 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:MLR)
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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