Hexagen 皮肤
K号: K171191 · 2017-08-25
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器械摘要
Hexagen Derm is the device name listed in this FDA 510(k) record. The listed applicant is Global Health Solutions, LLC. It received FDA 510(k) clearance on 2017-08-25 under 510(k) number K171191. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.
常见问题
What is the Hexagen Derm?
Hexagen Derm is a medical device that received FDA 510(k) clearance on 2017-08-25. The listed applicant is Global Health Solutions, LLC. The 510(k) number is K171191.
When did Hexagen Derm receive FDA 510(k) clearance?
Hexagen Derm received FDA 510(k) clearance on 2017-08-25, under 510(k) number K171191.
Who is the listed applicant for Hexagen Derm?
The FDA 510(k) record lists Global Health Solutions, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Hexagen Derm?
The FDA product code for Hexagen Derm is FRO. This falls under the Anesthesiology category.
相关临床试验
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。
列明Global Health Solutions, LLC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。
相关器械（代码：FRO）
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。
K254168Actolind®（06.3637. Actolind®凝胶加强型）ACTO GmbHK254041SkinSmart 抗菌保湿凝胶Magic Science Supply, LLCK261646Redermax® 抗菌伤口基质Beijing Kreate Medical Co., Ltd.K253665Vashe Plus 抗菌溶液Urgo Medical North America, LLCK251929SilverCeuticals® 抗菌伤口凝胶Silverceuticals, Inc.K261023Microdacyn 伤口冲洗溶液Sonoma Pharmaceuticals, Inc.
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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