510(k) K051889
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