The following data is part of a premarket notification filed by Aspect Medical Systems, Inc. with the FDA for Bis Engine.
Device ID | K002837 |
510k Number | K002837 |
Device Name: | BIS ENGINE |
Classification | Index-generating Electroencephalograph Software |
Applicant | ASPECT MEDICAL SYSTEMS, INC. 141 NEEDHAM ST. Newton, MA 02464 |
Contact | Christine M Vozella |
Correspondent | Christine M Vozella ASPECT MEDICAL SYSTEMS, INC. 141 NEEDHAM ST. Newton, MA 02464 |
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 | 2000-09-12 |
Decision Date | 2000-09-19 |