System, laser, photodynamic therapy
PMA Number: P990021 · 2022-03-02
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Device Summary
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
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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