The following data is part of a premarket notification filed by Aspect Medical Systems, Inc. with the FDA for Eeg Monitor With Bis, Model A-2000.
Device ID | K030267 |
510k Number | K030267 |
Device Name: | EEG MONITOR WITH BIS, MODEL A-2000 |
Classification | Index-generating Electroencephalograph Software |
Applicant | ASPECT MEDICAL SYSTEMS, INC. 141 NEEDHAM ST. Newton, MA 02464 |
Contact | Christine Vozella |
Correspondent | Christine Vozella ASPECT MEDICAL SYSTEMS, INC. 141 NEEDHAM ST. Newton, MA 02464 |
Product Code | OLW |
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 | 2003-01-27 |
Decision Date | 2004-01-15 |
Summary: | summary |