Generator, shock-wave, for pain relief
PMA Number: P080028 · 2020-02-05
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Device Summary
Frequently Asked Questions
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.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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