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510(k) Data Aggregation

K Number

Device Name

VITAJET

Manufacturer

VITAJET CORP.

Date Cleared

1996-12-10

(158 days)

Product Code

KZE

Regulation Number

880.5430

Why did this record match?

Applicant Name (Manufacturer) :

VITAJET CORP.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized

Intended Use

Device Description

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