The following data is part of a premarket notification filed by Aspect Medical Systems, Inc. with the FDA for Modification To Eeg Monitor With Bis, Model A-2000.
| Device ID | K031694 |
| 510k Number | K031694 |
| Device Name: | MODIFICATION TO EEG MONITOR WITH BIS, MODEL A-2000 |
| Classification | Index-generating Electroencephalograph Software |
| Applicant | ASPECT MEDICAL SYSTEMS, INC. 1775 ROCKIES COURT Lafayette, CO 80026 |
| Contact | Christine Vozella |
| Correspondent | Christine Vozella ASPECT MEDICAL SYSTEMS, INC. 1775 ROCKIES COURT Lafayette, CO 80026 |
| 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 | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-06-02 |
| Decision Date | 2003-08-29 |
| Summary: | summary |