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The MyPathAdvantage test provides information about the bacterial, fungal, and protozoan communities present in the vaginal microbiome. It is performed by PathAdvantage, a CLIA-certified and CAP-accredited laboratory, using an Analyte Specific Reagent that has been determined by the FDA to not require clearance or approval. This test is intended for clinical use and should be interpreted by a qualified healthcare professional. The results may assist in identifying potential imbalances in the vaginal microbiome. This test does not diagnose, treat, or cure any medical condition. Treatment decisions should always be made in consultation with your physician, considering your individual medical history and other relevant factors.

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