FDA 510(k) Applications Submitted by KEVIN BOWDEN
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K960995 |
03/12/1996 |
CPR BIO-BARRIER FACESHEILD |
O-TWO SYSTEMS INTL., INC. |
K991195 |
04/08/1999 |
CAREVENT BLS, CAREVENT BLS+, CAREVENT ALS, CAREVENT ALS+, AND CAREVENT ATV |
O-TWO SYSTEMS INTL., INC. |
K021328 |
04/26/2002 |
SMART BAG MO |
O-TWO SYSTEMS INTERNATIONAL INC. |
K983643 |
10/16/1998 |
GENESIS BLS |
O-TWO SYSTEMS INTL., INC. |
K983705 |
10/21/1998 |
EMT RESUSCITATOR |
O-TWO SYSTEMS INTL., INC. |
K983785 |
10/27/1998 |
AUTOVENT 1000 |
O-TWO SYSTEMS INTL., INC. |
K983857 |
11/02/1998 |
AUTOVENT 1500 |
O-TWO SYSTEMS INTL., INC. |
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