FDA 510(k) Applications Submitted by NEALIE HARTMAN

FDA 510(k) Number Submission Date Device Name Applicant
K040066 01/13/2004 SIREMOBILE C06 SIEMENS MEDICAL SOLUTIONS USA, INC.
K040347 02/12/2004 SIREMOBIL ISO-C 3D SIEMENS MEDICAL SYSTEMS, INC.
K040577 03/04/2004 SOMATOM PROJECT P30L SIEMENS MEDICAL SYSTEMS, INC.
K041111 04/28/2004 MAGNETOM C! MR SYSTEM SIEMENS MEDICAL SOLUTIONS USA, INC.
K041112 04/28/2004 MAGNETOM ESPREE SYSTEM SIEMENS MEDICAL SOLUTIONS USA, INC.
K032280 07/24/2003 SIREMOBIL ISO-C 3D SIEMENS AG
K032428 07/29/2003 MAGNETOM AVANTO MR SYSTEM SIEMENS MEDICAL SOLUTIONS USA, INC.
K032475 08/12/2003 SOMATON COMPUTED TOMOGRAPHY X-RAY SYSTEMS SLIDING GANTRY OPTION SIEMENS MEDICAL SOLUTIONS USA, INC.
K042229 08/17/2004 SOMATOM RADIATION TREATMENT PLANNING (RTP) PACKAGE SIEMENS MEDICAL SOLUTION, INC. USA
K042328 08/27/2004 SOMATOM SPIRIT SIEMENS MEDICAL SYSTEMS, INC.
K042617 09/24/2004 31P/1H HEADCOIL FOR MAGNETOM ALLEGRA SIEMENS MEDICAL SOLUTIONS USA INC.
K042718 09/30/2004 13C/1H OCCIPITAL HEADCOIL FOR MAGNETOM ALLEGRA SIEMENS MEDICAL SOLUTIONS, INC.
K033238 10/06/2003 MOBILETTE XP AND MOBILETT XPHYBRID SIEMENS MEDICAL SYSTEMS, INC.
K043030 11/03/2004 MAGNETOM C! MR SYSTEM SIEMENS MEDICAL SOLUTIONS
K040665 03/04/2004 SOMATOM SENSATION 64 AND SENSATION CARDIAC SIEMENS MEDICAL SOLUTIONS USA, INC.
K032536 08/18/2003 SOMATOM EXTENDED FIELD OF VIEW SOFTWARE OPTION SIEMENS MEDICAL SOLUTIONS USA, INC.


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