Stent, urethral, prostatic, semi-permanent
PMA Number: P060010 · 2022-10-07
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Device Summary
Frequently Asked Questions
What is the Stent, urethral, prostatic, semi-permanent?
Stent, urethral, prostatic, semi-permanent is a medical device that received FDA 510(k) clearance on 2022-10-07. The listed applicant is Srs Medical.
When did Stent, urethral, prostatic, semi-permanent receive FDA 510(k) clearance?
The clearance date for Stent, urethral, prostatic, semi-permanent can be found in the official FDA records.
Who is the listed applicant for Stent, urethral, prostatic, semi-permanent?
The FDA 510(k) record lists Srs Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Stent, urethral, prostatic, semi-permanent?
The FDA product code for Stent, urethral, prostatic, semi-permanent is NZC.
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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