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510(k) Data Aggregation

K Number

Device Name

THE LEADAWAY

Manufacturer

THERAPY EQUIPMENT, INC.

Date Cleared

1999-10-13

(90 days)

Product Code

IKD

Regulation Number

890.1175

Why did this record match?

Applicant Name (Manufacturer) :

THERAPY EQUIPMENT, INC.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized

Intended Use

The Leadaway is to be used as a lead wire for electrotherapy devices.

Device Description

Not Found

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