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510(k) Data Aggregation

K Number

Device Name

MULTI-TEST II

Manufacturer

LINCOLN DIAGNOSTICS, INC.

Date Cleared

1996-08-07

(82 days)

Product Code

SCL, LDH

Regulation Number

880.5570

Why did this record match?

Applicant Name (Manufacturer) :

LINCOLN DIAGNOSTICS, INC.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized

Intended Use

The sole indication for Multi-Test II is for the percutaneous administration of diagnostic allergenic extracts.

Device Description

Not Found

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