BioMin Restore Plus
K号: K200077 · 2020-11-06
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决定日期2020-11-06
产品代码LBH
咨询委员会DE
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器械摘要
BioMin Restore Plus is the device name listed in this FDA 510(k) record. The listed applicant is Dr. Collins, Inc.. It received FDA 510(k) clearance on 2020-11-06 under 510(k) number K200077. The device is classified under product code LBH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the BioMin Restore Plus?
BioMin Restore Plus is a medical device that received FDA 510(k) clearance on 2020-11-06. The listed applicant is Dr. Collins, Inc.. The 510(k) number is K200077.
When did BioMin Restore Plus receive FDA 510(k) clearance?
BioMin Restore Plus received FDA 510(k) clearance on 2020-11-06, under 510(k) number K200077.
Who is the listed applicant for BioMin Restore Plus?
The FDA 510(k) record lists Dr. Collins, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BioMin Restore Plus?
The FDA product code for BioMin Restore Plus is LBH.
相关临床试验
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列明Dr. Collins, 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：LBH）
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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