510(k) K051469

CAREVENT ATV+ AND CAREVENT MRI by O-Two Medical Technologies, Inc. — Product Code BTL

K051469 is an FDA 510(k) premarket notification submitted by O-Two Medical Technologies, Inc. for the device "CAREVENT ATV+ AND CAREVENT MRI". The FDA issued a decision of Substantially Equivalent on September 28, 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
September 28, 2005
Date Received
June 3, 2005
Clearance Type
Traditional
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