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510(k) Data Aggregation

K Number

Device Name

NICCHECK I

Manufacturer

DYNAGEN, INC.

Date Cleared

1996-12-13

(88 days)

Product Code

MRS

Regulation Number

862.3220

Why did this record match?

Applicant Name (Manufacturer) :

DYNAGEN, INC.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized

Intended Use

Device Description

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