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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