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510(k) Data Aggregation

K Number

Device Name

ANCURE SHEATH MODEL # 40315, 40320, 40325

Manufacturer

GUIDANT CARDIAC AND VASCULAR SURGERY

Date Cleared

2002-01-24

(402 days)

Product Code

Regulation Number

Type

Panel

Reference & Predicate Devices

N/A

Why did this record match?

Device Name :

ANCURE SHEATH MODEL # 40315, 40320, 40325

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

AI/ML Overview

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