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510(k) Data Aggregation

K Number

Device Name

EPI 2

Manufacturer

UNIVERSAL H.R. SYSTEM, INC.

Date Cleared

1997-02-11

(1169 days)

Product Code

KCX

Regulation Number

878.5360

Why did this record match?

Applicant Name (Manufacturer) :

UNIVERSAL H.R. SYSTEM, INC.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized

Intended Use

Device Description

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