FDA 510(k) Applications Submitted by James Bonds

FDA 510(k) Number Submission Date Device Name Applicant
K050072 01/12/2005 GOODKNIGHT 425ST NELLCOR PURITAN BENNETT, INC.
K070408 02/12/2007 DURAMAX REUSABLE OXIMETRY SENSOR NELLCOR PURITAN BENNETT, INC.
K020940 03/22/2002 SUPERSTITCH VASCULAR SUTURING DEVICE, 6 FRENCH, MODELS 06-15-00X; MID-LENGTH 06-25-00X SUTURA, INC.
K110923 04/01/2011 COBAS 4800 CT / NG TEST ROCHE MOLECULAR SYSTEMS, INC.
K070899 04/02/2007 PURITAN BENNETT LEGENDAIR XL2 NELLCOR PURITAN BENNETT
K031470 05/09/2003 PURITAN BENNETT, GOODKNIGHT 420 EVOLUTION, MODEL M-113903-US TYCO HEALTHCARE NANCY
K221433 05/17/2022 Facet 28G Universal Lancet Facet Technologies LLC
K071575 06/08/2007 SANDMAN INTRO MALLINCKRODT DEVELOPPEMENT FRANCE
K022103 06/28/2002 PURITAN-BENNETT 700 RENAISSANCE II SPIROMETRY SYSTEM PURITAN BENNETT CORP.
K041819 07/06/2004 GOODKNIGHT 425, MODELM-114500-00 MALLINCKRODT DEVELOPPEMENT FRANCE
K222539 08/22/2022 Facet Blood Lancets Facet Technologies LLC
K012865 08/27/2001 SUPERSTITCH VASCULAR SUTURING DEVICE SUTURA, INC.
K223099 09/30/2022 Facet Manatee Reusable Lancing Base Facet Technologies LLC
K223370 11/04/2022 NeatNick Heel Safety Lancet Facet Technologies LLC
K063501 11/20/2006 KNIGHTCONTROL REMOTE CONTROL, MODEL M-114700-US MALLINCKRODT DEVELOPPEMENT FRANCE
K053388 12/05/2005 MODEL 840 VENTILATOR WITH PROPORTIONAL ASSIST VENTILATION PLUS SOFTWARE OPTION PURITAN BENNETT CORP.


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