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FDA PMA

Assays to detect pre-existing antibodies to adeno-associated virus (AAV) viral vectors

PMA Number: P250002 · 2025-07-24

ApplicantQuest Diagnostics Nichols Institute
Decision Date2025-07-24
PMA NumberP250002
Product CodeQWQ
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeHE

Device Summary

Assays to detect pre-existing antibodies to adeno-associated virus (AAV) viral vectors is the device name listed in this FDA 510(k) record. The listed applicant is Quest Diagnostics Nichols Institute. It received FDA 510(k) clearance on 2025-07-24. The device is classified under product code QWQ. It was reviewed by the HE advisory panel.

Frequently Asked Questions

What is the Assays to detect pre-existing antibodies to adeno-associated virus (AAV) viral vectors?

Assays to detect pre-existing antibodies to adeno-associated virus (AAV) viral vectors is a medical device that received FDA 510(k) clearance on 2025-07-24. The listed applicant is Quest Diagnostics Nichols Institute.

When did Assays to detect pre-existing antibodies to adeno-associated virus (AAV) viral vectors receive FDA 510(k) clearance?

The clearance date for Assays to detect pre-existing antibodies to adeno-associated virus (AAV) viral vectors can be found in the official FDA records.

Who is the listed applicant for Assays to detect pre-existing antibodies to adeno-associated virus (AAV) viral vectors?

The FDA 510(k) record lists Quest Diagnostics Nichols Institute as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Assays to detect pre-existing antibodies to adeno-associated virus (AAV) viral vectors?

The FDA product code for Assays to detect pre-existing antibodies to adeno-associated virus (AAV) viral vectors is QWQ.

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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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