Provicol QM Plus
K号: K161630 · 2016-09-15
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器械摘要
Provicol QM Plus is the device name listed in this FDA 510(k) record. The listed applicant is Voco GmbH. It received FDA 510(k) clearance on 2016-09-15 under 510(k) number K161630. The device is classified under product code EMB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Provicol QM Plus?
Provicol QM Plus is a medical device that received FDA 510(k) clearance on 2016-09-15. The listed applicant is Voco GmbH. The 510(k) number is K161630.
When did Provicol QM Plus receive FDA 510(k) clearance?
Provicol QM Plus received FDA 510(k) clearance on 2016-09-15, under 510(k) number K161630.
Who is the listed applicant for Provicol QM Plus?
The FDA 510(k) record lists Voco GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Provicol QM Plus?
The FDA product code for Provicol QM Plus is EMB.
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列明Voco GmbH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。
官方来源
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