MC1 Plus
K号: K161502 · 2016-08-16
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决定日期2016-08-16
产品代码IMI
咨询委员会PM
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决定实质等同
器械摘要
MC1 Plus is the device name listed in this FDA 510(k) record. The listed applicant is General Project S.R.L.. It received FDA 510(k) clearance on 2016-08-16 under 510(k) number K161502. The device is classified under product code IMI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the MC1 Plus?
MC1 Plus is a medical device that received FDA 510(k) clearance on 2016-08-16. The listed applicant is General Project S.R.L.. The 510(k) number is K161502.
When did MC1 Plus receive FDA 510(k) clearance?
MC1 Plus received FDA 510(k) clearance on 2016-08-16, under 510(k) number K161502.
Who is the listed applicant for MC1 Plus?
The FDA 510(k) record lists General Project S.R.L. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MC1 Plus?
The FDA product code for MC1 Plus is IMI.
相关器械（代码：IMI）
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官方来源
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