SnugKap
K号: K193383 · 2021-06-07
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决定日期2021-06-07
产品代码MVA
咨询委员会NE
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决定实质等同
器械摘要
SnugKap is the device name listed in this FDA 510(k) record. The listed applicant is Headstart, Ltd.. It received FDA 510(k) clearance on 2021-06-07 under 510(k) number K193383. The device is classified under product code MVA. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the SnugKap?
SnugKap is a medical device that received FDA 510(k) clearance on 2021-06-07. The listed applicant is Headstart, Ltd.. The 510(k) number is K193383.
When did SnugKap receive FDA 510(k) clearance?
SnugKap received FDA 510(k) clearance on 2021-06-07, under 510(k) number K193383.
Who is the listed applicant for SnugKap?
The FDA 510(k) record lists Headstart, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SnugKap?
The FDA product code for SnugKap is MVA.
相关临床试验
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相关器械（代码：MVA）
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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