The following data is part of a premarket notification filed by Siemens Life Support Systems with the FDA for Anesthesia Workstation.
Device ID | K901474 |
510k Number | K901474 |
Device Name: | ANESTHESIA WORKSTATION |
Classification | Cabinet, Table And Tray, Anesthesia |
Applicant | SIEMENS LIFE SUPPORT SYSTEMS 2360 N. PALMER DR. Schaumburg, IL 60173 |
Contact | Ellen Farney |
Correspondent | Ellen Farney SIEMENS LIFE SUPPORT SYSTEMS 2360 N. PALMER DR. Schaumburg, IL 60173 |
Product Code | BRY |
CFR Regulation Number | 868.6100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-03-27 |
Decision Date | 1990-04-10 |