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FDA PMA

Optoacoustic Imaging System

PMA Number: P200003 · 2022-06-17

ApplicantSeno Medical Instruments, Inc.
Decision Date2022-06-17
PMA NumberP200003
Product CodeQNK
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeRA

Device Summary

Optoacoustic Imaging System is the device name listed in this FDA 510(k) record. The listed applicant is Seno Medical Instruments, Inc.. It received FDA 510(k) clearance on 2022-06-17. The device is classified under product code QNK. It was reviewed by the RA advisory panel.

Frequently Asked Questions

What is the Optoacoustic Imaging System?

Optoacoustic Imaging System is a medical device that received FDA 510(k) clearance on 2022-06-17. The listed applicant is Seno Medical Instruments, Inc..

When did Optoacoustic Imaging System receive FDA 510(k) clearance?

The clearance date for Optoacoustic Imaging System can be found in the official FDA records.

Who is the listed applicant for Optoacoustic Imaging System?

The FDA 510(k) record lists Seno Medical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Optoacoustic Imaging System?

The FDA product code for Optoacoustic Imaging System is QNK.

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.

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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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