FDA 510(k) Applications Submitted by Meryl Koch

FDA 510(k) Number Submission Date Device Name Applicant
K140362 02/12/2014 KATALYST REVOLVER LASER PROBES, KATALYST REVOLVER ILLUMINATED LASER PROBES, KATALYST REVOLVER ILLUMINATED PROBES KATALYST SURGICAL, LLC
K141781 07/02/2014 KOGENT SPETZLER LIGHTED SUCTION TUBES KATALYST SURGICAL, LLC
K163632 12/22/2016 Katalyst Cyclophotocoagulation Probe Katalyst Surgical, LLC
K192963 10/23/2019 Kogent Torus Ultrasonic Aspirator Katalyst Surgical, LLC


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