Steritec Products, Inc. is one of 21805 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Steritec Products, Inc. - FDA 510(k) Cleared Devices
Recent clearances: EMU-GRAPH 4 EMULATOR, MODEL CI 144, INSTANT READOUT CHEMICAL INTEGRATOR CHALLENGE PACK, MODEL LT- 105, STERITEC CONTAINER CORD - CI 135, STERITEC PROCESS INDICATOR LABELS - CI 140, STERITEC PROCESS INDICATOR DOTS - CI 137
12
Total
12
Cleared
0
Denied
Steritec Products, Inc. has 12 FDA 510(k) cleared general hospital devices. Based in Castle Rock, US.
Historical record: 12 cleared submissions from 2000 to 2009.
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) Regulatory Record - Steritec Products, Inc.
12 devices
Cleared
Mar 05, 2009
EMU-GRAPH 4 EMULATOR, MODEL CI 144
General Hospital
86d
Cleared
Aug 15, 2008
INSTANT READOUT CHEMICAL INTEGRATOR CHALLENGE PACK, MODEL LT- 105
General Hospital
206d
Cleared
Oct 03, 2005
STERITEC CONTAINER CORD - CI 135, STERITEC PROCESS INDICATOR LABELS - CI 140,...
General Hospital
19d
Cleared
Sep 09, 2004
STERITEC EMU-GRAPH, MODEL NO. CI 131/US
General Hospital
155d
Cleared
Aug 11, 2003
BOWIE-DICK MINI PAK, MODEL BD 115
General Hospital
230d
Cleared
Mar 04, 2002
INTEGRAPH FLASH, MODEL CI 110
General Hospital
200d
Cleared
Aug 06, 2001
CROSS-CHECKS DUAL, MODEL CI 125
General Hospital
164d
Cleared
Feb 07, 2001
CROSS-CHECKS LF, MODEL CI 119/S &CI 119/L
General Hospital
83d
Cleared
Dec 08, 2000
STERILIZATION PROCESS INDICATOR TAPES MODEL CI112 & CI123
General Hospital
73d
Cleared
Nov 29, 2000
EO GAS STERILIZATION PROCESS INDICATOR TAPES, MODEL CI 124
General Hospital
77d
Cleared
Jun 23, 2000
STERITEC AUTOCLAVE TAPES, MODEL CI122 & CI1234
General Hospital
24d
Cleared
May 15, 2000
STERITEC STEAM BIOLOGICAL TEST PACK WITH INSTANT READOUT INTEGRATOR, MODEL BI...
General Hospital
7d