510(k) K123125
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