FDA 510(k) Applications Submitted by STERITEC PRODUCTS, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K080136 01/22/2008 INSTANT READOUT CHEMICAL INTEGRATOR CHALLENGE PACK, MODEL LT- 105 STERITEC PRODUCTS, INC.
K010534 02/23/2001 CROSS-CHECKS DUAL, MODEL CI 125 STERITEC PRODUCTS, INC.
K040901 04/07/2004 STERITEC EMU-GRAPH, MODEL NO. CI 131/US STERITEC PRODUCTS, INC.
K001444 05/08/2000 STERITEC STEAM BIOLOGICAL TEST PACK WITH INSTANT READOUT INTEGRATOR, MODEL BI 103 STERITEC PRODUCTS, INC.
K001649 05/30/2000 STERITEC AUTOCLAVE TAPES, MODEL CI122 & CI1234 STERITEC PRODUCTS, INC.
K012732 08/16/2001 INTEGRAPH FLASH, MODEL CI 110 STERITEC PRODUCTS, INC.
K002861 09/13/2000 EO GAS STERILIZATION PROCESS INDICATOR TAPES, MODEL CI 124 STERITEC PRODUCTS, INC.
K052516 09/14/2005 STERITEC CONTAINER CORD - CI 135, STERITEC PROCESS INDICATOR LABELS - CI 140, STERITEC PROCESS INDICATOR DOTS - CI 137 STERITEC PRODUCTS, INC.
K003002 09/26/2000 STERILIZATION PROCESS INDICATOR TAPES MODEL CI112 & CI123 STERITEC PRODUCTS, INC.
K003533 11/16/2000 CROSS-CHECKS LF, MODEL CI 119/S &CI 119/L STERITEC PRODUCTS, INC.
K083650 12/09/2008 EMU-GRAPH 4 EMULATOR, MODEL CI 144 STERITEC PRODUCTS, INC.
K024293 12/24/2002 BOWIE-DICK MINI PAK, MODEL BD 115 STERITEC PRODUCTS, INC.


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