Kit, rna detection, human papillomavirus
PMA Number: P120007 · 2026-02-03
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Device Summary
Frequently Asked Questions
What is the Kit, rna detection, human papillomavirus?
Kit, rna detection, human papillomavirus is a medical device that received FDA 510(k) clearance on 2026-02-03. The listed applicant is Gen-Probe Incorporated.
When did Kit, rna detection, human papillomavirus receive FDA 510(k) clearance?
The clearance date for Kit, rna detection, human papillomavirus can be found in the official FDA records.
Who is the listed applicant for Kit, rna detection, human papillomavirus?
The FDA 510(k) record lists Gen-Probe Incorporated as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Kit, rna detection, human papillomavirus?
The FDA product code for Kit, rna detection, human papillomavirus is OYB.
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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