Physiometrix, Inc.
FDA 510(k) medical device clearances.
Top product codes for Physiometrix, Inc.
Recent clearances by Physiometrix, Inc.
- K051874 — SEDLINE SEDATION MONITOR WITH FRONTAL PSI AND SEDTRACE EEG ELECTROSE SET
- K033999 — SEDLINE WITH FRONTAL PSI
- K020670 — MODEL 4310 PSARRAY2 EEG ELECTRODE
- K020671 — PSA4000 EEG MONITOR WITH FRONTAL PSI
- K001069 — MODEL 4000 EEG MONITOR WITH PSI (PSA4000)
- K001055 — MODEL 4300 PSARRAY EEG ELECTRODE SET
- K970942 — MODEL 1320, NEUROLINK II NEUROMONITORING SYSTEM
- K970694 — MODEL 1700, HYDRO PREP
- K962447 — EQUINOX DIGITAL EEG SYSTEM
- K962157 — MODEL 1310 NEUROLINK NEUROMONITORING SYSTEM
- K961609 — MODEL 1220, OR E-NET (54-62 CM)
- K960873 — MODEL 1210, MEDIUM E-NET
- K960885 — MODEL 1240, SMALL E NET
- K960732 — HYDROSPOT EEG ELECTRODE MODEL 1501, HYDROSPOT LEADWIRE MODEL 1500
- K953449 — MODEL 1207, HYDRODOT NEUROMONITORING SYSTEM ADHESIVE PADS
- K946318 — MODEL 1001, HYDRODOT(TM) NEUROMONITORING SYSTEM WITH E NET(TM) EEG INTERFACE CABLE
- K934505 — TRIGEL MULTIFUNCTION ELECTRODE
- K940219 — TRIGEL- MULTIFUNCTION ELECTRODE
- K935260 — PHYSIOMETRIX CABLE ADAPTER MODIFICATION
- K930080 — E*NET NEUROMONITORING SYSTEM
- K931885 — DRIGEL MULTIFUNCTION ELECTRODE
- K921207 — DRIGEL DEFIBRILLATOR/SYNCHRONIZED COARDIOVERSION
Data sourced from openFDA. This site is unofficial and independent of the FDA.