Steritec Products, Inc.
Steritec Products, Inc. holds FDA 510(k) medical device clearances, first cleared 2000, most recent 2009.
Top product codes for Steritec Products, Inc.
Recent clearances by Steritec Products, Inc.
- K083650 — EMU-GRAPH 4 EMULATOR, MODEL CI 144
- K080136 — INSTANT READOUT CHEMICAL INTEGRATOR CHALLENGE PACK, MODEL LT- 105
- K052516 — STERITEC CONTAINER CORD - CI 135, STERITEC PROCESS INDICATOR LABELS - CI 140, STERITEC PROCESS INDICATOR DOTS - CI 137
- K040901 — STERITEC EMU-GRAPH, MODEL NO. CI 131/US
- K024293 — BOWIE-DICK MINI PAK, MODEL BD 115
- K012732 — INTEGRAPH FLASH, MODEL CI 110
- K010534 — CROSS-CHECKS DUAL, MODEL CI 125
- K003533 — CROSS-CHECKS LF, MODEL CI 119/S &CI 119/L
- K003002 — STERILIZATION PROCESS INDICATOR TAPES MODEL CI112 & CI123
- K002861 — EO GAS STERILIZATION PROCESS INDICATOR TAPES, MODEL CI 124
- K001649 — STERITEC AUTOCLAVE TAPES, MODEL CI122 & CI1234
- K001444 — STERITEC STEAM BIOLOGICAL TEST PACK WITH INSTANT READOUT INTEGRATOR, MODEL BI 103
Data sourced from openFDA. This site is unofficial and independent of the FDA.