510(k) K051889

CAREVENT CA AND DRA by O-Two Medical Technologies, Inc. — Product Code BTL

K051889 is an FDA 510(k) premarket notification submitted by O-Two Medical Technologies, Inc. for the device "CAREVENT CA AND DRA". The FDA issued a decision of Substantially Equivalent on August 30, 2005. The device falls under product code BTL (Ventilator, Emergency, Powered (Resuscitator)), a Class II device regulated under 21 CFR 868.5925. O-Two Medical Technologies, Inc. has at least 7 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 30, 2005
Date Received
July 12, 2005
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Ventilator, Emergency, Powered (Resuscitator)
Device Class
Class II
Regulation Number
868.5925
Review Panel
AN
Submission Type