FDA 510(k)

Jabra Enhance Plus

K号: K213424 · 2022-01-19

决定日期2022-01-19

产品代码QDD

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

Jabra Enhance Plus is the device name listed in this FDA 510(k) record. The listed applicant is GN Hearing A/S. It received FDA 510(k) clearance on 2022-01-19 under 510(k) number K213424. The device is classified under product code QDD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Jabra Enhance Plus?

Jabra Enhance Plus is a medical device that received FDA 510(k) clearance on 2022-01-19. The listed applicant is GN Hearing A/S. The 510(k) number is K213424.

When did Jabra Enhance Plus receive FDA 510(k) clearance?

Jabra Enhance Plus received FDA 510(k) clearance on 2022-01-19, under 510(k) number K213424.

Who is the listed applicant for Jabra Enhance Plus?

The FDA 510(k) record lists GN Hearing A/S as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Jabra Enhance Plus?

The FDA product code for Jabra Enhance Plus is QDD.

列明GN Hearing A/S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。

K254108Jabra Enhance Select 自适应型（Jabra Enhance Select 550）K193303耳鸣声发生器模块 K180495耳鸣声发生器模块 K181586耳鸣声发生器模块

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。