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510(k) Data Aggregation

K Number

Device Name

PROACT 1

Manufacturer

PROACT CO.

Date Cleared

2001-06-13

(176 days)

Product Code

IRP

Regulation Number

890.5650

Why did this record match?

Applicant Name (Manufacturer) :

PROACT CO.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized

Intended Use

Device Description

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