Sterilucent, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Sterilucent, Inc. has 7 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 7 cleared submissions from 2014 to 2019. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Sterilucent, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Sterilucent, Inc.
7 devices
Cleared
Oct 22, 2019
Sterilucent self-Contained Biological Indicator, Sterilucent Lumen Cycle...
General Hospital
88d
Cleared
Oct 21, 2019
Sterilucent VH2O2 Chemical Indicators
General Hospital
87d
Cleared
Sep 13, 2019
Sterilucent HC 80TT Hydrogen Peroxide Sterilizer
General Hospital
254d
Cleared
Jan 20, 2015
STERILUCENT STERILIZATION CONTAINER SYSTEM
General Hospital
169d
Cleared
Nov 03, 2014
STERILUCENT SELF-CONTAINED BIOLOGICAL INDICATOR
General Hospital
174d
Cleared
Oct 31, 2014
STERILUCENT PSD-85 HYDROGEN PEROXIDE STERILIZER
General Hospital
249d
Cleared
Oct 31, 2014
STERILUCENT PROCESS CHALLENGE DEVICE
General Hospital
164d