The following data is part of a premarket notification filed by Physiometrix, Inc. with the FDA for Sedline With Frontal Psi.
| Device ID | K033999 |
| 510k Number | K033999 |
| Device Name: | SEDLINE WITH FRONTAL PSI |
| Classification | Index-generating Electroencephalograph Software |
| Applicant | PHYSIOMETRIX, INC. FIVE BILLERICA PARK, 101 BILLERICA AVE. North Billerica, MA 01862 |
| Contact | Dawn E Frazer |
| Correspondent | Dawn E Frazer PHYSIOMETRIX, INC. FIVE BILLERICA PARK, 101 BILLERICA AVE. North Billerica, MA 01862 |
| Product Code | OLW |
| Subsequent Product Code | OLT |
| Subsequent Product Code | OMC |
| Subsequent Product Code | ORT |
| CFR Regulation Number | 882.1400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-12-24 |
| Decision Date | 2004-02-06 |
| Summary: | summary |