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Raydiant Oximetry Secures FDA Approval for Lumerah Investigational Device Exemption (IDE) Study

SAN RAMON, Calif., April 10, 2024 (GLOBE NEWSWIRE) Raydiant Oximetry, Inc., a clinical-stage medical device company that develops medical tec.

United statesEastern virginia medical schoolElizabeth cherotNeilp rayRaydiant lumerahGeorge saadeInnovation fundDrug administrationRaydiant oximetry incNational institutes of healthDean for women healthUnited states foodInvestigational device exemptionEarly feasibility studyRaydiant oximetryDevice designation

CONCEPT MEDICAL RECEIVES US FDA IDE APPROVAL FOR MAGICTOUCH AVF INDICATION, THEIR FIFTH US CLINICAL STUDY APPROVAL FOR THE MAGICTOUCH PORTFOLIO

CONCEPT MEDICAL RECEIVES US FDA IDE APPROVAL FOR MAGICTOUCH AVF INDICATION, THEIR FIFTH US CLINICAL STUDY APPROVAL FOR THE MAGICTOUCH PORTFOLIO
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United statesManish doshiDrug administrationConcept medicalArteriovenous fistulaChronic renalInvestigational device exemptionMagictouch sirolimus coated balloon

AngioDynamics (ANGO) Receives 510(k) Clearance for AlphaVac F18 System

AngioDynamics (ANGO) Receives 510(k) Clearance for AlphaVac F18 System
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United statesWilliam brent keelingJuan carlos sernaJohnm moriartyMona ranadeEmory university school of medicineAngiodynamics incDrug administrationPulmonary embolism response teamDepartment of surgeryDavid geffen school of medicineClinical affairsUnited states foodAngiodynamics senior vice presidentAcute pulmonary embolism extraction trialAlphavac system

AngioDynamics Receives 510(k) Clearance for AlphaVac F1885 System in Treatment of PE

New Indication for Treatment of Pulmonary Embolism Enhances Device Utility in Critical Medical Scenarios .

United statesWilliam brent keelingJuan carlos sernaMona ranadeMachanahalli balakrishnaAmerican heart associationDavid geffen school of medicineDepartment of surgeryClinical affairsPulmonary embolism response teamAngiodynamics incDrug administrationEmory university school of medicineUnited states foodAngiodynamics senior vice presidentAcute pulmonary embolism extraction trial

Concept Medical receives US FDA IDE approval for MagicTouch AVF indication, their fifth US clinical study approval for the MagicTouch portfolio

Concept Medical receives US FDA IDE approval for MagicTouch AVF indication, their fifth US clinical study approval for the MagicTouch portfolio
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United statesManish doshiDrug administrationConcept medicalArteriovenous fistulaChronic renalInvestigational device exemptionMagictouch sirolimus coated balloon