Nutrifill
K号: K181566 · 2018-10-22
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决定日期2018-10-22
产品代码MRC
咨询委员会OP
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决定实质等同
器械摘要
Nutrifill is the device name listed in this FDA 510(k) record. The listed applicant is Contamac, Ltd.. It received FDA 510(k) clearance on 2018-10-22 under 510(k) number K181566. The device is classified under product code MRC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Nutrifill?
Nutrifill is a medical device that received FDA 510(k) clearance on 2018-10-22. The listed applicant is Contamac, Ltd.. The 510(k) number is K181566.
When did Nutrifill receive FDA 510(k) clearance?
Nutrifill received FDA 510(k) clearance on 2018-10-22, under 510(k) number K181566.
Who is the listed applicant for Nutrifill?
The FDA 510(k) record lists Contamac, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Nutrifill?
The FDA product code for Nutrifill is MRC.
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列明Contamac, Ltd.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。
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相关器械（代码：MRC）
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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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