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510(k) Data Aggregation

K Number

Device Name

CORELIFE

Manufacturer

CORE HEALTHCARE LTD.

Date Cleared

1997-07-24

(274 days)

Product Code

Regulation Number

Why did this record match?

Applicant Name (Manufacturer) :

CORE HEALTHCARE LTD.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty

Intended Use

This device is used to inject fluids into or withdraw fluids from the body.

Device Description

CORELIFE (PISTON SYRINGE)

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