SBB

System, Colorectal Neoplasia, Rna Markers And Hemoglobin Detection

Product code
SBB
Device name
System, Colorectal Neoplasia, Rna Markers And Hemoglobin Detection
Device class
Class 3
Medical specialty
Unknown
Marketing pathway
PMA

FDA classification definition

The colorectal neoplasia RNA and hemoglobin assay is a non-invasive, qualitative in vitro diagnostic intended for the detection of colorectal neoplasia associated RNA markers and for the presence of occult hemoglobin in human stool. The test is to aid in the detection of colorectal cancer (CRC) and advanced adenomas (AA). The test is not a replacement for diagnostic colonoscopy. It is indicated for use in adults 45 years or older, who are typical average-risk candidates for colorectal cancer (CRC) screening. A positive result may indicate the presence of CRC or AA and should be followed by a diagnostic colonoscopy.

Definition text from the FDA device classification database (U.S. federal government work, public domain).

Official FDA classification page: SBB
Classification and pathway per current FDA publications. Data from openFDA (CC0).