Steritec Products Mfg Co, Inc. - FDA 510(k) Cleared Devices
22
Total
22
Cleared
0
Denied
Steritec Products Mfg Co, Inc. has 22 FDA 510(k) cleared general hospital devices. Based in Castle Rock, US.
Historical record: 22 cleared submissions from 1996 to 2020.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Steritec Products Mfg Co, Inc.
22 devices
Cleared
May 21, 2020
Getinge Assured MI Steam Migrating Integrator
General Hospital
108d
Cleared
Aug 27, 2014
STERITEC BIOLOGICAL TEST PACK WITH INSTANT READOUT INTEGRATOR
General Hospital
281d
Cleared
Aug 25, 2014
STERITEC SMART-READ BIOLOGICAL TEST PACK WITH INSTANT READOUT INTEGRATOR
General Hospital
300d
Cleared
Nov 26, 2013
STERITEC GREEN CARD PACK BOWIE-DICK TEST
General Hospital
119d
Cleared
Apr 30, 2013
STERITEC GREEN CARD PACK BOWIE-DICK TEST MODEL BD 126
General Hospital
218d
Cleared
Dec 12, 2012
STERITEC LEAD FREE STERILIZATION PROCESS INDICATOR TAPE
General Hospital
112d
Cleared
Jul 08, 2011
STERITEC SMART-READ BIOLOGICAL TEST PACK WITH INSTANT READOUT INTEGRATOR
General Hospital
74d
Cleared
Feb 11, 2011
SMART READ BIOLOGICAL TEST PACK
General Hospital
126d
Cleared
Apr 30, 2008
EMU-GRAPH EMULATOR, MODEL CI 131
General Hospital
247d
Cleared
Mar 14, 2000
STEAM/EO RECORD CARD, MODEL CI 121
General Hospital
28d
Cleared
Jun 10, 1999
STERI-PAK LF BOWIE-DICK TEST PACK
General Hospital
135d
Cleared
Nov 20, 1998
STERI-PAK BOWIE DICK TEST PACK
General Hospital
151d