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510(k) Data Aggregation

K Number

Device Name

HYDROBRUSH (TM) KERATOME

Manufacturer

Date Cleared

1998-01-23

(305 days)

Product Code

Regulation Number

Why did this record match?

Applicant Name (Manufacturer) :

MEDJET, INC.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty

Intended Use

Any condition which requires removal of the epithelium from the cornea.

Device Description

Not Found

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