FDA 510(k) Applications Submitted by PHYSIOMETRIX, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K960732 02/22/1996 HYDROSPOT EEG ELECTRODE MODEL 1501, HYDROSPOT LEADWIRE MODEL 1500 PHYSIOMETRIX, INC.
K970694 02/25/1997 MODEL 1700, HYDRO PREP PHYSIOMETRIX, INC.
K020670 03/01/2002 MODEL 4310 PSARRAY2 EEG ELECTRODE PHYSIOMETRIX, INC.
K020671 03/01/2002 PSA4000 EEG MONITOR WITH FRONTAL PSI PHYSIOMETRIX, INC.
K960873 03/04/1996 MODEL 1210, MEDIUM E-NET PHYSIOMETRIX, INC.
K960885 03/04/1996 MODEL 1240, SMALL E NET PHYSIOMETRIX, INC.
K970942 03/14/1997 MODEL 1320, NEUROLINK II NEUROMONITORING SYSTEM PHYSIOMETRIX, INC.
K001055 04/03/2000 MODEL 4300 PSARRAY EEG ELECTRODE SET PHYSIOMETRIX, INC.
K001069 04/03/2000 MODEL 4000 EEG MONITOR WITH PSI (PSA4000) PHYSIOMETRIX, INC.
K961609 04/25/1996 MODEL 1220, OR E-NET (54-62 CM) PHYSIOMETRIX, INC.
K962157 06/04/1996 MODEL 1310 NEUROLINK NEUROMONITORING SYSTEM PHYSIOMETRIX, INC.
K962447 06/24/1996 EQUINOX DIGITAL EEG SYSTEM PHYSIOMETRIX, INC.
K051874 07/11/2005 SEDLINE SEDATION MONITOR WITH FRONTAL PSI AND SEDTRACE EEG ELECTROSE SET PHYSIOMETRIX, INC.
K033999 12/24/2003 SEDLINE WITH FRONTAL PSI PHYSIOMETRIX, INC.


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