FDA 510(k) Applications Submitted by THOMAS J ENGLISH

FDA 510(k) Number Submission Date Device Name Applicant
K020022 01/03/2002 DINAMAP PRO SERIES MONITOR, MODELS 110, 210, 310, 410 GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES
K992638 08/06/1999 DINAMAP PRO SERIES MONITOR, MODELS 100, 200, 300, 400 CRITIKON COMPANY,LLC
K014255 12/26/2001 DINAMAP PROCARE SERIES MONITOR; MODEL 100, 200, 300, 400 GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES
K990352 02/05/1999 COULTER AC T DIFF 2 ANALYZER COULTER CORP.
K000500 02/14/2000 DINAMAP ADVANCED NIBP MODULE CRITIKON COMPANY, L.L.C.
K991070 03/31/1999 COULTER Z2 ANALYZER COULTER CORP.
K971469 04/22/1997 COULTER ACT TRON CELL CONTROL COULTER CORP.
K002248 07/25/2000 DINAMAP PRO 1000 MONITOR, MODEL 1000 CRITIKON COMPANY,LLC
K962988 08/01/1996 COULTER GEN-S SYSTEM COULTER CORP.
K012915 08/30/2001 DINAMAP PRO 1000 MONITOR, MODEL 1000 GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES
K973634 09/24/1997 COULTER AC.T DIFF ANALYZER COULTER CORP.
K964988 12/13/1996 COULTER AC.T SERIES ANALYZER COULTER CORP.


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