Physiometrix, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Physiometrix, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SEDLINE SEDATION MONITOR WITH FRONTAL PSI AND SEDTRACE EEG ELECTROSE SET, SEDLINE WITH FRONTAL PSI, MODEL 4310 PSARRAY2 EEG ELECTRODE
22
Total
22
Cleared
0
Denied
Physiometrix, Inc. has 22 FDA 510(k) cleared neurology devices. Based in Sunnyvale, US.
Historical record: 22 cleared submissions from 1992 to 2005.
Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Physiometrix, Inc.
22 devices
Cleared
Sep 02, 2005
SEDLINE SEDATION MONITOR WITH FRONTAL PSI AND SEDTRACE EEG ELECTROSE SET
Neurology
53d
Cleared
Feb 06, 2004
SEDLINE WITH FRONTAL PSI
Neurology
44d
Cleared
Oct 08, 2002
MODEL 4310 PSARRAY2 EEG ELECTRODE
Neurology
221d
Cleared
Oct 04, 2002
PSA4000 EEG MONITOR WITH FRONTAL PSI
Neurology
217d
Cleared
Jun 30, 2000
MODEL 4000 EEG MONITOR WITH PSI (PSA4000)
Neurology
88d
Cleared
May 11, 2000
MODEL 4300 PSARRAY EEG ELECTRODE SET
Neurology
38d
Cleared
Jun 02, 1997
MODEL 1320, NEUROLINK II NEUROMONITORING SYSTEM
Neurology
80d
Cleared
May 14, 1997
MODEL 1700, HYDRO PREP
Neurology
78d
Cleared
Dec 12, 1996
EQUINOX DIGITAL EEG SYSTEM
Neurology
171d
Cleared
Nov 25, 1996
MODEL 1310 NEUROLINK NEUROMONITORING SYSTEM
Neurology
174d
Cleared
May 10, 1996
MODEL 1220, OR E-NET (54-62 CM)
Neurology
15d
Cleared
Apr 26, 1996
MODEL 1210, MEDIUM E-NET
Neurology
53d