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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