FDA 510(k) Applications Submitted by RICHARD DEMELLO

FDA 510(k) Number Submission Date Device Name Applicant
K070502 02/21/2007 RADIUS SNARE RADIUS MEDICAL TECHNOLOGIES, INC.
K160664 03/09/2016 Aqueduct 100 Cervical Dilator GTIMD LLC
K130714 03/15/2013 PROGIGY SUPPORT CATHETER RADIUS MEDICAL, LLC
K192019 07/29/2019 Dragonfly OpStarÖ Imaging Catheter, AptiVueÖ Software version E.5.1 Abbott Medical


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