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FDA 510(k)

LigaSure Impact Curved, Large Jaw, Open Sealer/Divider, Nano-coated

K号: K162047 · 2016-09-15

申请人Covidien
决定日期2016-09-15
产品代码GEI
咨询委员会SU
决定Substantially Equivalent

器械摘要

LigaSure Impact Curved, Large Jaw, Open Sealer/Divider, Nano-coated is the device name listed in this FDA 510(k) record. The listed applicant is Covidien. It received FDA 510(k) clearance on 2016-09-15 under 510(k) number K162047. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the LigaSure Impact Curved, Large Jaw, Open Sealer/Divider, Nano-coated?

LigaSure Impact Curved, Large Jaw, Open Sealer/Divider, Nano-coated is a medical device that received FDA 510(k) clearance on 2016-09-15. The listed applicant is Covidien. The 510(k) number is K162047.

When did LigaSure Impact Curved, Large Jaw, Open Sealer/Divider, Nano-coated receive FDA 510(k) clearance?

LigaSure Impact Curved, Large Jaw, Open Sealer/Divider, Nano-coated received FDA 510(k) clearance on 2016-09-15, under 510(k) number K162047.

Who is the listed applicant for LigaSure Impact Curved, Large Jaw, Open Sealer/Divider, Nano-coated?

The FDA 510(k) record lists Covidien as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LigaSure Impact Curved, Large Jaw, Open Sealer/Divider, Nano-coated?

The FDA product code for LigaSure Impact Curved, Large Jaw, Open Sealer/Divider, Nano-coated is GEI.

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相关器械(代码:GEI)

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。

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