Cytomegalovirus (cmv) dna quantitative assay
PMA Number: P210029 · 2024-10-23
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Device Summary
Frequently Asked Questions
What is the Cytomegalovirus (cmv) dna quantitative assay?
Cytomegalovirus (cmv) dna quantitative assay is a medical device that received FDA 510(k) clearance on 2024-10-23. The listed applicant is Hologic, Inc..
When did Cytomegalovirus (cmv) dna quantitative assay receive FDA 510(k) clearance?
The clearance date for Cytomegalovirus (cmv) dna quantitative assay can be found in the official FDA records.
Who is the listed applicant for Cytomegalovirus (cmv) dna quantitative assay?
The FDA 510(k) record lists Hologic, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Cytomegalovirus (cmv) dna quantitative assay?
The FDA product code for Cytomegalovirus (cmv) dna quantitative assay is PAB.
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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