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FDA PMA

用于疼痛缓解的冲击波发生器

PMA编号:P080028 · 2020-02-05

决定日期2020-02-05
PMA 编号P080028
产品代码NBN
设备分类第3类
医疗专科U
咨询委员会SU 请注意,您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。

器械摘要

Generator, shock-wave, for pain relief is the device name listed in this FDA 510(k) record. The listed applicant is Storz Medical AG. It received FDA 510(k) clearance on 2020-02-05. The device is classified under product code NBN. It was reviewed by the SU advisory panel.

常见问题

What is the Generator, shock-wave, for pain relief?

Generator, shock-wave, for pain relief is a medical device that received FDA 510(k) clearance on 2020-02-05. The listed applicant is Storz Medical AG.

When did Generator, shock-wave, for pain relief receive FDA 510(k) clearance?

The clearance date for Generator, shock-wave, for pain relief can be found in the official FDA records.

Who is the listed applicant for Generator, shock-wave, for pain relief?

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

What is the FDA product code for Generator, shock-wave, for pain relief?

The FDA product code for Generator, shock-wave, for pain relief is NBN.

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