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510(k) Data Aggregation

K Number

Validate with FDA (Live)

Device Name

Luja female (20051); Luja female (20052); Luja female (20054); Luja female (20056)

Manufacturer

Date Cleared

2024-07-26

(102 days)

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Panel

Gastroenterology/Urology

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AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

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