FDA 510(k) Applications Submitted by CALVIN D OSTLER
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K100474 |
02/18/2010 |
QUICKLASEDUAL+, QUICKLASE810, QUICKLASE810, QUICKLASE980, QUICKLASE980 MODEL: 3W,5W,3W,5W |
QUICKLASE LIMITED |
K970637 |
02/20/1997 |
ACCUCURE 1000 |
LASERMED, INC. |
K992061 |
06/18/1999 |
PULSTAR |
LASERMED, INC. |
K072995 |
10/23/2007 |
TWINWAVE DENTAL LASER, TIDALWAVE 810 DENTAL LASER, TIDALWAVE 980 DENTAL LASER |
LUMEN DEVELOPMENT AND MANUFACTURING, INC. |
K964486 |
11/08/1996 |
ACCUCURE 3000 |
LASERMED, INC. |
|
|