FDA 510(k) Applications for Medical Device Product Code "OVY"

FDA 510(k) Number Applicant Device Name Decision Date
DEN110002 STERIS Corporation SYSTEM 1E PROCESS BIOLOGICAL MONITORING KIT 03/30/2012
K180553 Steris Corporation VERIFY Spore Test Strip for S40 Sterilant 05/29/2018
K231746 Steris Corporation VERIFY Spore Test Strip for S40 Sterilant Concentrate 09/11/2023


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