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510(k) Data Aggregation

K Number

Device Name

ELITE ELECTROMED L.I.T.E. 4/1

Manufacturer

ELITE ELECTROMEDICAL

Date Cleared

2006-03-15

(89 days)

Product Code

Regulation Number

Why did this record match?

Applicant Name (Manufacturer) :

ELITE ELECTROMEDICAL

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty

Intended Use

THE L.I.T.E. 4/1 IS INDICATED FOR THE TREATMENT OF NECK AND SHOULDER PAIN OF MUSCULOSKELET OF ORIGIN.

Device Description

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