The following data is part of a premarket notification filed by Ge Healthcare Finland Oy with the FDA for Ge Datex-ohmeda S/5 Adu Carestation.
Device ID | K090892 |
510k Number | K090892 |
Device Name: | GE DATEX-OHMEDA S/5 ADU CARESTATION |
Classification | Gas-machine, Anesthesia |
Applicant | GE HEALTHCARE FINLAND OY 3030 OHMEDA DRIVE PO BOX 7550 Madison, WI 53707 -7550 |
Contact | Adrienne Lenz |
Correspondent | Adrienne Lenz GE HEALTHCARE FINLAND OY 3030 OHMEDA DRIVE PO BOX 7550 Madison, WI 53707 -7550 |
Product Code | BSZ |
CFR Regulation Number | 868.5160 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2009-03-31 |
Decision Date | 2009-04-30 |
Summary: | summary |