FDA 510(k) Applications Submitted by JOHN R SCOVILLE

FDA 510(k) Number Submission Date Device Name Applicant
K070461 02/16/2007 VERIFY STEAM INDICATORS, MODELS 250F 25, 250F 30, 270F 15, 270F 3-10 AND 270F 4 STERIS Corporation
K080750 03/17/2008 BROWNE RAPICIDE GLUTARALDEHYDE INDICATOR STERIS Corporation
K070895 03/30/2007 VERIFY CHALLENGE PACKS, MODELS 270F 4 CHALLENGE PACK; 275F 3 CHALLENGE PACK; 275F 10 CHALLENGE PACK STERIS Corporation
K081600 06/06/2008 STERIS RESERT XL TEST STRIP STERIS Corporation
K071895 07/09/2007 VERIFY 275 DEGREE F. 3-10 INDICATOR; 10 INDICATOR; 3 INDICATOR STERIS Corporation
K072072 07/30/2007 HARMONY LED-1 SURGICAL LIGHTING SYSTEM STERIS Corporation
K073683 12/28/2007 VERIFY CHALLENGE PACKS - VERSION 2 STERIS Corporation
K091022 04/09/2009 MODIFICATION TO RESERT XL HLD HIGH LEVEL DISINFECTANT STERIS Corporation
K090514 02/26/2009 VERIFY SELF-CONTAINED BIOLOGICAL INDICATOR FOR VAPORIZED (VH2O2) STERILIZATION PROCESSES STERIS Corporation
K071087 04/17/2007 VIS-U-ALL II HEAT-SEAL POUCH AND TUBING STERIS Corporation
K102275 08/11/2010 THERMEDX 37-5 ELECTROCAUTERY PROBES, MODELS MPJ200, MPJ210, MPS220, MPN230, BPH240 THERMEDX, LLC
K083097 10/17/2008 AMSCO V-PRO 1 LOW TEMPERATURE STERILIZATION SYSTEM STERIS Corporation
K073244 11/19/2007 VERIFY SELF-CONTAINED BIOLOGICAL INDICATOR FOR VH202 GASEOUS STERILIZATION PROCESSES STERIS Corporation
K073618 12/26/2007 VERIFY SIRIUS BIOLOGICAL INDICATOR CHALLENGE PACK STERIS Corporation
K080420 02/15/2008 RESERT XL HLD HIGH LEVEL DISINFECTANT STERIS Corporation
K090136 01/21/2009 STERIS CMAX XLT SURGICAL TABLE STERIS Corporation
K072510 09/06/2007 VERIFY V-PRO CHEMICAL INDICATOR, VERSIONS 1 AND 2 STERIS Corporation
K090371 02/13/2009 VIS-U-ALL LOW TEMPERATURE TYVEK STERILIZATION POUCH FOR V-PRO 1 STERILIZATION SYSTEM STERIS Corporation
K083643 12/09/2008 VERIFY 275F GRAVITY INDICATORS STERIS Corporation
K083665 12/10/2008 VERIFY SCBI 275F 3-10 STERIS Corporation


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