FDA 510(k) Applications Submitted by Katrin Svensson

FDA 510(k) Number Submission Date Device Name Applicant
K110193 01/24/2011 FEMOSTOP PLYS, FEMOSTOP HD, FEMOSTOP COMPRESSION ARCH; FEMOSTOP II PLUS SET; FEMOSTOP II PLUS ARCH, BILATERAL ADAPTER; F ST. JUDE MEDICAL SYSTEMS AB
K181756 07/02/2018 Gangi-SoftGuard Coaxial Needle, Gangi-HydroGuard Coaxial Needle AprioMed AB
K193268 11/26/2019 APrioCore Plus AprioMed AB


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