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510(k) Data Aggregation

K Number

Device Name

PHERON PERIPHERAL PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) CATHETER

Manufacturer

BIOTRONIK AG

Date Cleared

2005-10-28

(28 days)

Product Code

LIT

Regulation Number

870.1250

Why did this record match?

Applicant Name (Manufacturer) :

BIOTRONIK AG

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized

Intended Use

Device Description

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