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FDA PMA

System, laser, photodynamic therapy

PMA Number: P990021 · 2022-03-02

Decision Date2022-03-02
PMA NumberP990021
Product CodeMVF
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeSU

Device Summary

System, laser, photodynamic therapy is the device name listed in this FDA 510(k) record. The listed applicant is Pinnacle Biologics, Inc.. It received FDA 510(k) clearance on 2022-03-02. The device is classified under product code MVF. It was reviewed by the SU 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 2022-03-02. The listed applicant is Pinnacle Biologics, Inc..

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 Pinnacle Biologics, Inc. 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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