510(k) Report

FDA product code · Microbiology

Device To Detect Or Measure Nucleic Acid From Viruses Associated With Head And Neck Cancers

OJYClass II21 CFR 866.3236510(k) required1 decision since 20200 recalls

1 FDA decision since 2020. No recall names this code.

A device to detect or measure nucleic acid from viruses associated with head and neck cancers is an in vitro diagnostic test for prescription use in the detection of viral nucleic acid in nasopharyngeal or oropharyngeal cellular specimens from patients with signs and symptoms of head and neck cancer. The test result is intended to be used in conjunction with other clinical information to aid in assessing the…

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026 Download the data (CSV)

FIG. A — Illustration, microbiology panel

Twenty years of OJY at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.

FDA decisions per year · OJY

1in 2020

2020: 1
2007high 1 (2020) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OJY

Too few OJY 510(k)s in any year since 2007 to give a median.

Recalls per year · OJY

No recall names OJY since 2007.

Adverse event reports per year · OJY

No MAUDE report names OJY since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20201—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—
FIG. 1 — OJY by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in OJY? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

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