D-Clip；D-Clip施用器
K号: K180757 · 2019-04-12
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决定日期2019-04-12
产品代码HCH
咨询委员会NE
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决定实质等同
器械摘要
D-Clip; D-Clip Applier is the device name listed in this FDA 510(k) record. The listed applicant is Peter Lazic GmbH. It received FDA 510(k) clearance on 2019-04-12 under 510(k) number K180757. The device is classified under product code HCH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the D-Clip; D-Clip Applier?
D-Clip; D-Clip Applier is a medical device that received FDA 510(k) clearance on 2019-04-12. The listed applicant is Peter Lazic GmbH. The 510(k) number is K180757.
When did D-Clip; D-Clip Applier receive FDA 510(k) clearance?
D-Clip; D-Clip Applier received FDA 510(k) clearance on 2019-04-12, under 510(k) number K180757.
Who is the listed applicant for D-Clip; D-Clip Applier?
The FDA 510(k) record lists Peter Lazic GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for D-Clip; D-Clip Applier?
The FDA product code for D-Clip; D-Clip Applier is HCH.
相关临床试验
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相关器械（代码：HCH）
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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