510(k) Predicate Finder
Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.
Let the assistant find your predicates
Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.
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Device To Detect Or Measure Nucleic Acid From Viruses Associated With Head And Neck Cancers
Microbiology
The Device to Detect or Measure Nucleic Acid from Viruses Associated with Head and Neck Cancers is a prescription-use in vitro diagnostic test that detects viral nucleic acid (such as HPV or EBV) in nasopharyngeal or oropharyngeal cellular specimens from patients with signs and symptoms of head and neck cancer, intended to aid clinicians in assessing clinical status or the likelihood of virus-associated head and neck cancer in conjunction with other clinical information. Classified as FDA Class 2 under regulation 21 CFR 866.3236 within the Microbiology medical specialty, it requires a 510(k) premarket notification. The product code is OJY. It is not flagged as an implant or life-sustaining device.
510(k) Clearances
1 matchesWhat is a Predicate Device?
A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.
Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.
Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.