FDA 510(k) Applications Submitted by JUDI HOFFMAN

FDA 510(k) Number Submission Date Device Name Applicant
K020353 02/04/2002 OMNIA X/XS ULTRASOUND SYSTEM SIEMENS MEDICAL SYSTEMS, INC.
K951999 04/28/1995 HOLOPSY SYSTEM NEOVISION CORP.
K001400 05/03/2000 ELEGRA MILLENNIUM ENHANCED DIAGNOSTIC ULTRASOUND SYSTEM SIEMENS MEDICAL SOLUTIONS USA, INC.
K033196 10/02/2003 SONOLINE ANTARES WITH CLARIFY VE SIEMENS MEDICAL SOLUTIONS USA, INC.
K003125 10/05/2000 SONOLINE ELEGRA DIAGNOSTIC ULTRASOUND SYSTEM SIEMENS MEDICAL SOLUTIONS USA, INC.
K023720 11/05/2002 SONOLINE ANTARES ULTRASOUND SYSTEM SIEMENS MEDICAL SOLUTIONS USA, INC.


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