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Magnolia Medical Expands Steripath® Micro Initial Specimen Diversion Device® (ISDD®) Product Family with New FDA 510(k) Clearance

/PRNewswire/ Magnolia Medical Technologies, Inc., announced today U.S. Food and Drug Administration (FDA) 510(k) clearance of 19 new Steripath® Micro.

Greg bullingtonLaboratory standards instituteDrug administrationPrnewswire magnolia medical technologies incClinical laboratoryNational email update to cliniciansEmergency nurses associationSteripath microMedical technologiesInitial specimen diversionMagnolia medicalInitial specimen diversion deviceMicro initial specimen diversionSteripath initial specimen diversion deviceClinical performance guaranteeCulture contamination prevention actions

Magnolia Medical Awarded National GPO and Value-Based Contract from Premier Inc for Steripath® Initial Specimen Diversion Device®

/PRNewswire/ Magnolia Medical Technologies, Inc., inventors of Steripath®, the only FDA 510(k)-cleared device platform indicated to reduce blood culture.

Bob gerberichPrnewswire magnolia medical technologies incMedical technologiesPremier incMicro initial specimen diversion deviceClinical performanceValue based tierNow steripathMagnolia medicalClinical performance guaranteeInitial specimen diversion techniqueMagnolia medical technologies

Magnolia Medical Awarded National GPO and Value-Based Contract from Premier Inc for Steripath® Initial Specimen Diversion Device®

/PRNewswire/ Magnolia Medical Technologies, Inc., inventors of Steripath®, the only FDA 510(k)-cleared device platform indicated to reduce blood culture.

Bob gerberichPrnewswire magnolia medical technologies incMedical technologiesPremier incMicro initial specimen diversion deviceClinical performanceValue based tierNow steripathMagnolia medicalClinical performance guaranteeInitial specimen diversion techniqueMagnolia medical technologies

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