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510(k) Data Aggregation

K Number

Device Name

CEBE

Manufacturer

Date Cleared

1997-06-24

(50 days)

Product Code

Regulation Number

Why did this record match?

Applicant Name (Manufacturer) :

SUUNTO USA

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty

Intended Use

Eye Protection against ultra violet radiation.

Device Description

CEBE SUNGLASSES

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