FDA 510(k) Applications Submitted by Scott Thiel

FDA 510(k) Number Submission Date Device Name Applicant
K080227 01/30/2008 ACCU-CHEK 360 DIABETES MANAGEMENT SYSTEM ROCHE DIAGNOSTICS CORP.
K070585 03/01/2007 ACCU-CHEK PERFORMA SYSTEM ROCHE DIAGNOSTICS CORP.
K060620 03/08/2006 ACCU-CHEK AVIVA TEST STRIPS ROCHE DIAGNOSTICS CORP.
K100704 03/12/2010 ACCU-CHEK FLEXLINK PLUS INFUSION SET, ACCU-CHECK LINKASSIST PLUS INSERTION DEVICE DISETRONIC MEDICAL SYSTEMS AG
K050760 03/24/2005 ACCU-CHEK POCKET COMPASS DIABETES MANAGEMENT SOFTWARE ROCHE DIAGNOSTICS CORP.
K040796 03/29/2004 ACCU-CHEK GO SYSTEM ROCHE DIAGNOSTICS CORP.
K060876 03/31/2006 ACCU-CHEK INSULIN PUMP CONFIGURATION SOFTWARE (STANDARD), MODEL 04625137001; ACCU-CHEK INSULIN PUMP CONFIGURATION SOFTWA DISETRONIC MEDICAL SYSTEMS AG
K050872 04/06/2005 ACCU-CHEK INTEGRA SYSTEM ROCHE DIAGNOSTICS CORP.
K101196 04/29/2010 ACCU-CHEK ULTRFLEX INFUSION SET ROCHE DIAGNOSTICS CORP.
K021513 05/09/2002 ACCU-CHEK ADVANTAGE MODULE ROCHE DIAGNOSTICS CORP.
K111353 05/16/2011 ACCU-CHECK COMBO SYSTEM Roche Diagnostics
K081389 05/19/2008 ACCU-CHEK COMPACT PLUS BLOOD GLUCOSE MONITORING SYSTEM Roche Diagnostics
K031755 06/06/2003 ACCU-CHEK COMPACT TEST STRIP ROCHE DIAGNOSTICS CORP.
K022171 07/03/2002 ACCU-CHEK COMPACT SYSTEM ROCHE DIAGNOSTICS CORP.
K062395 08/16/2006 ACCU-CHEK SMART PIX ROCHE DIAGNOSTICS CORP.
K032552 08/19/2003 ACCU-CHEK ADVANTAGE SYSTEM ROCHE DIAGNOSTICS CORP.
K082595 09/08/2008 MODIFICATION TO:ACCU-CHEK POCKET COMPASS DIABETES MANAGEMENT SOFTWARE Roche Diagnostics
K063146 10/16/2006 ACCU-CHEK LINKASSIST DISETRONIC MEDICAL SYSTEMS AG
K042887 10/19/2004 ACCU-CHEK SPIRIT DISETRONIC MEDICAL SYSTEMS AG
K043000 11/01/2004 MODIFICATION TO D-TRONPLUS DISETRONIC MEDICAL SYSTEMS AG
K043474 12/16/2004 ACCU-CHEK AVIVA SYSTEM ROCHE DIAGNOSTICS CORP.
K014139 12/17/2001 DIABETES ASSISTANT SOFTWARE ROCHE DIAGNOSTICS CORP.
K043529 12/21/2004 ACCU-CHEK ADVISOR INSULIN GUIDANCE SOFTWARE ROCHE DIAGNOSTICS CORP.


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