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510(k) Data Aggregation

K Number

Validate with FDA (Live)

Device Name

AT HOME DRUG TEST, MODEL 9078 T

Manufacturer

Date Cleared

2001-04-05

(31 days)

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AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

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