The following data is part of a premarket notification filed by Siemens Life Support Systems with the FDA for Pcm Anesthesia.
Device ID | K903991 |
510k Number | K903991 |
Device Name: | PCM ANESTHESIA |
Classification | Gas-machine, 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 | BSZ |
CFR Regulation Number | 868.5160 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-08-29 |
Decision Date | 1991-02-25 |