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510(k) Data Aggregation
K Number
K133351Device Name
NEXUS NIS-6P LUER ACTIVATED DEVICE
Manufacturer
Date Cleared
2014-05-22
(203 days)
Product Code
Regulation Number
880.5440Why did this record match?
Applicant Name (Manufacturer) :
NEXUS MEDICAL LLC
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
The Nexus NIS®-6P is a pressure-rated, luer-activated, normally closed, bidirectional, neutral pressure device intended for use as an accessory to an IV catheter placed in the vein or artery for intravenous administration of blood, IV drugs and IV fluids to the patient including neonatal, pediatric and immunocompromised patients. The Nexus NIS®-6P may also be safely used with power injectors at 10mL/sec and pressures up to 325 psi. The Nexus NIS®-6P has a pre-slit septum which does not require the use of a stainless steel needle and passively aids in the reduction of needlestick injuries.
Device Description
The Nexus NIS®-6P is a pressure-rated, luer-activated, normally closed, bidirectional, neutral pressure device. It has a pre-slit septum which does not require the use of a stainless steel needle.
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