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FDA 510(k)

Cochlear Baha 6 Max声音处理器,Cochlear Baha适配软件6,Cochlear Baha智能应用

K号: K202048 · 2021-02-23

决定日期2021-02-23
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

Cochlear Baha 6 Max Sound Processor, Cochlear Baha Fitting Software 6, Cochlear Baha Smart App is the device name listed in this FDA 510(k) record. The listed applicant is Cochlear Americas. It received FDA 510(k) clearance on 2021-02-23 under 510(k) number K202048. 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 Cochlear Baha 6 Max Sound Processor, Cochlear Baha Fitting Software 6, Cochlear Baha Smart App?

Cochlear Baha 6 Max Sound Processor, Cochlear Baha Fitting Software 6, Cochlear Baha Smart App is a medical device that received FDA 510(k) clearance on 2021-02-23. The listed applicant is Cochlear Americas. The 510(k) number is K202048.

When did Cochlear Baha 6 Max Sound Processor, Cochlear Baha Fitting Software 6, Cochlear Baha Smart App receive FDA 510(k) clearance?

Cochlear Baha 6 Max Sound Processor, Cochlear Baha Fitting Software 6, Cochlear Baha Smart App received FDA 510(k) clearance on 2021-02-23, under 510(k) number K202048.

Who is the listed applicant for Cochlear Baha 6 Max Sound Processor, Cochlear Baha Fitting Software 6, Cochlear Baha Smart App?

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

What is the FDA product code for Cochlear Baha 6 Max Sound Processor, Cochlear Baha Fitting Software 6, Cochlear Baha Smart App?

The FDA product code for Cochlear Baha 6 Max Sound Processor, Cochlear Baha Fitting Software 6, Cochlear Baha Smart App 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Cochlear Americas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。

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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。

官方来源

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