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FDA PRODUCT CODE · CLASS II

PQAVaginitis And Bacterial Vaginosis Nucleic Acid Detection System

A vaginitis and bacterial vaginosis nucleic acid detection system is a qualitative in vitro diagnostic device for the direct detection of nucleic acid sequences from microorganisms associated with vaginitis or bacterial vaginosis. The device is indicated for individuals with signs and symptoms of vaginitis or bacterial vaginosis and aids in the diagnosis of these vaginal infections.

DEVICE CLASS
Class II
REGULATION
21 CFR 866.3975
MEDICAL SPECIALTY
Microbiology
REVIEW PANEL
MI
ImplantLife-sustainingGMP-exemptThird-party review eligible
3
510(K)/PMA CLEARANCES
510k: 3
0
RECALL ENTRIES

Recent clearances

K260021Roche Molecular Systems, Inc. · 510k2026-07-16
K243725Becton, Dickinson and Company · 510k2024-12-19
K243345Hologic, Inc. · 510k2024-11-25

Related on SPEQ

Medical devices industryMedical device quality (ISO 13485)FDA device clearancesFDA enforcement & recalls

Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

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