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FDA PMA

System, Colorectal Neoplasia, RNA Markers and Hemoglobin detection

PMA Number: P230001 · 2026-09-08

Decision Date2026-09-08
PMA NumberP230001
Product CodeSBB
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteePA

Device Summary

System, Colorectal Neoplasia, RNA Markers and Hemoglobin detection is the device name listed in this FDA 510(k) record. The listed applicant is Geneoscopy, Inc.. It received FDA 510(k) clearance on 2026-09-08. The device is classified under product code SBB. It was reviewed by the PA advisory panel.

Frequently Asked Questions

What is the System, Colorectal Neoplasia, RNA Markers and Hemoglobin detection?

System, Colorectal Neoplasia, RNA Markers and Hemoglobin detection is a medical device that received FDA 510(k) clearance on 2026-09-08. The listed applicant is Geneoscopy, Inc..

When did System, Colorectal Neoplasia, RNA Markers and Hemoglobin detection receive FDA 510(k) clearance?

The clearance date for System, Colorectal Neoplasia, RNA Markers and Hemoglobin detection can be found in the official FDA records.

Who is the listed applicant for System, Colorectal Neoplasia, RNA Markers and Hemoglobin detection?

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

What is the FDA product code for System, Colorectal Neoplasia, RNA Markers and Hemoglobin detection?

The FDA product code for System, Colorectal Neoplasia, RNA Markers and Hemoglobin detection is SBB.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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