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510(k) Data Aggregation

K Number

Device Name

VENISECT LASER LANCET

Manufacturer

VENISECT, INC.

Date Cleared

1997-04-11

(486 days)

Product Code

GEX

Regulation Number

878.4810

Why did this record match?

Applicant Name (Manufacturer) :

VENISECT, INC.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized

Intended Use

Device Description

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