FDA 510(k)ADHEAR 系统
K号: K172460 · 2018-04-27
决定日期2018-04-27
产品代码LXB
咨询委员会医疗设备监管文本描述翻译如下:
关于[公司/产品名称]的监管信息:
- 美国食品药品监督管理局(FDA)批准号:[510(k)编号]
- 预市场批准(PMA)申请号:[PMA编号]
- 临床试验注册号(NCT):[NCT编号]
- 医学文献标识符(PMID):[PMID编号]
- 产品标识符:[标识符]
- 相关政策:医疗监管政策v1
- 更多信息请访问:[URL]
请注意,以上翻译保留了公司/产品名称、FDA、510(k)、PMA、NCT、PMID、标识符和URL。
决定实质等同
器械摘要
ADHEAR System is the device name listed in this FDA 510(k) record. The listed applicant is Med-El Elektromedizinische Geraete GmbH. It received FDA 510(k) clearance on 2018-04-27 under 510(k) number K172460. The device is classified under product code LXB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the ADHEAR System?
ADHEAR System is a medical device that received FDA 510(k) clearance on 2018-04-27. The listed applicant is Med-El Elektromedizinische Geraete GmbH. The 510(k) number is K172460.
When did ADHEAR System receive FDA 510(k) clearance?
ADHEAR System received FDA 510(k) clearance on 2018-04-27, under 510(k) number K172460.
Who is the listed applicant for ADHEAR System?
The FDA 510(k) record lists Med-El Elektromedizinische Geraete GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ADHEAR System?
The FDA product code for ADHEAR System is LXB.
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Med-El Elektromedizinische Geraete 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。
相关器械(代码:LXB)
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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