FDA 510(k) Applications Submitted by BOB ROSE
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K973299 |
09/02/1997 |
PIN CARE KIT |
BROWN MEDICAL INDUSTRIES |
K040234 |
02/02/2004 |
LASERPRO CO2 CARBON DIOXIDE LASER SYSTEM |
PHOTOMEDEX, INC. |
K040294 |
02/06/2004 |
LASERPRO DIODE LASER SYSTEMS, MODELS 810, 940 & 980 |
PHOTOMEDEX, INC. |
K020847 |
03/15/2002 |
XTRAC EXCIMER LASER SYSTEM, MODEL AL7000 |
PHOTO MEDEX, INC. |
K011382 |
05/07/2001 |
XTRAC EXCIMER LASER SYSTEM, MODEL AL 7000 |
PHOTO MEDEX, INC. |
K031451 |
05/07/2003 |
XTRACXL PLUS EXCIMER LASER SYSTEM, MODEL AL7000 |
PHOTO MEDEX, INC. |
K981898 |
06/01/1998 |
ORTHOVU-1000 |
MAGNEVU |
K051428 |
06/01/2005 |
VTRAC EXCIMER LAMP SYSTEM |
PHOTO MEDEX, INC. |
K041943 |
07/19/2004 |
XTRAC XL, MODEL AL8000 |
PHOTO MEDEX, INC. |
K042211 |
08/16/2004 |
MODIFICATION TO: LASERPRO 810, 940, AND 980 DIODE DIODE LASER SYSTEMS |
SURGICAL LASER TECHNOLOGIES, INC. |
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