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510(k) Data Aggregation

K Number

Device Name

GENESIS RMP

Manufacturer

TECAN U.S., INC.

Date Cleared

1997-03-18

(210 days)

Product Code

JRA

Regulation Number

862.2680

Why did this record match?

Product Code :

JRA

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized

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Device Description

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