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Found 2 results

510(k) Data Aggregation

K Number

Device Name

VIA 1-01 INFUSION PUMP/BLOOD CHEMISTRY SYSTEM

Manufacturer

VIA MEDICAL CORP.

Date Cleared

1996-12-05

(1098 days)

Product Code

CCE, CCC, LZF

Regulation Number

868.1200

Why did this record match?

Applicant Name (Manufacturer) :

VIA MEDICAL CORP.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized

Intended Use

Device Description

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K Number

Device Name

PUMP/BLOOD CHEMISTRY MONITOR

Manufacturer

VIA MEDICAL CORP.

Date Cleared

1996-02-28

(320 days)

Product Code

LZF

Regulation Number

880.5725

Why did this record match?

Applicant Name (Manufacturer) :

VIA MEDICAL CORP.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized

Intended Use

Device Description

Ask a Question

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