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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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