510(k) K012924

DATEX-OHMEDA TEC 7 ANESTHESIA VAPORIZER by Datex-Ohmeda, Inc. — Product Code CAD

K012924 is an FDA 510(k) premarket notification submitted by Datex-Ohmeda, Inc. for the device "DATEX-OHMEDA TEC 7 ANESTHESIA VAPORIZER". The FDA issued a decision of Substantially Equivalent on January 30, 2002. The device falls under product code CAD (Vaporizer, Anesthesia, Non-Heated), a Class II device regulated under 21 CFR 868.5880. Datex-Ohmeda, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 30, 2002
Date Received
August 31, 2001
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Vaporizer, Anesthesia, Non-Heated
Device Class
Class II
Regulation Number
868.5880
Review Panel
AN
Submission Type