510(k) K123125

GE DATEX-OHMEDA AVANCE CS2 by Datex-Ohmeda, Inc. — Product Code BSZ

K123125 is an FDA 510(k) premarket notification submitted by Datex-Ohmeda, Inc. for the device "GE DATEX-OHMEDA AVANCE CS2". The FDA issued a decision of Substantially Equivalent on February 6, 2013. The device falls under product code BSZ (Gas-Machine, Anesthesia), a Class II device regulated under 21 CFR 868.5160. Datex-Ohmeda, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 6, 2013
Date Received
October 4, 2012
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Gas-Machine, Anesthesia
Device Class
Class II
Regulation Number
868.5160
Review Panel
AN
Submission Type