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Test, Fluorescence In Situ Hybridization (Fish), For Bladder Cancer Detection And Monitoring For Recurrence

NSD · Class III — High Risk (PMA approval required, life-sustaining) · Unknown

Classification

FDA Product Code
NSD
Device class
Class III — High Risk (PMA approval required, life-sustaining)
Regulation
Review panel
PA
Medical specialty
Unknown
Submission type
2
GMP exempt
N
Life sustaining
N
Implant
N
Third-party review
N

Definition

In vitro diagnostic test to detect aneuploidy for chromosomes 3, 7, 17 and loss of the 9p21 locus via fluorescence in situ hybridization (fish) in urine specimens from persons suspected of having bladder cancer. It is an adjunctive test for initial diagnosis of transitional cell carcinoma in symptomatic patients and subsequently monitoring for tumor recurrence in patients previously diagnosed with bladder cancer.

Market data

Cleared 510(k) submissions
0
Registered establishments
2

Source

Authoritative
FDA Device Classification database
Machine
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