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510(k) Data Aggregation

K Number

Validate with FDA (Live)

Device Name

STYROFOAM CUTTERS FOR BLOCK CASTING SYSTEM

Manufacturer

ARPLAY MEDICAL S.A.

Date Cleared

2001-03-13

(64 days)

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Regulation Number

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Panel

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N/A

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AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

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