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FDA PMA

System, laser, photodynamic therapy

PMA Number: P050026 · 2025-02-11

Decision Date2025-02-11
PMA NumberP050026
Product CodeMVF
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeOP

Device Summary

System, laser, photodynamic therapy is the device name listed in this FDA 510(k) record. The listed applicant is Bausch + Lomb Ireland Limited. It received FDA 510(k) clearance on 2025-02-11. The device is classified under product code MVF. It was reviewed by the OP advisory panel.

Frequently Asked Questions

What is the System, laser, photodynamic therapy?

System, laser, photodynamic therapy is a medical device that received FDA 510(k) clearance on 2025-02-11. The listed applicant is Bausch + Lomb Ireland Limited.

When did System, laser, photodynamic therapy receive FDA 510(k) clearance?

The clearance date for System, laser, photodynamic therapy can be found in the official FDA records.

Who is the listed applicant for System, laser, photodynamic therapy?

The FDA 510(k) record lists Bausch + Lomb Ireland Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for System, laser, photodynamic therapy?

The FDA product code for System, laser, photodynamic therapy is MVF.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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