Vonflex S
K号: K152615 · 2016-11-03
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决定日期2016-11-03
产品代码ELW
咨询委员会DE
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决定实质等同
器械摘要
Vonflex S is the device name listed in this FDA 510(k) record. The listed applicant is Vericom Co., Ltd.. It received FDA 510(k) clearance on 2016-11-03 under 510(k) number K152615. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Vonflex S?
Vonflex S is a medical device that received FDA 510(k) clearance on 2016-11-03. The listed applicant is Vericom Co., Ltd.. The 510(k) number is K152615.
When did Vonflex S receive FDA 510(k) clearance?
Vonflex S received FDA 510(k) clearance on 2016-11-03, under 510(k) number K152615.
Who is the listed applicant for Vonflex S?
The FDA 510(k) record lists Vericom Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Vonflex S?
The FDA product code for Vonflex S is ELW.
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列明Vericom Co., Ltd.为申报人的其他记录
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相关器械（代码：ELW）
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