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FDA PMA

Stent, urethral, prostatic, semi-permanent

PMA Number: P060010 · 2022-10-07

ApplicantSrs Medical
Decision Date2022-10-07
PMA NumberP060010
Product CodeNZC
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeGU

Device Summary

Stent, urethral, prostatic, semi-permanent is the device name listed in this FDA 510(k) record. The listed applicant is Srs Medical. It received FDA 510(k) clearance on 2022-10-07. The device is classified under product code NZC. It was reviewed by the GU advisory panel.

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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