FDA 510(k) Applications Submitted by KAREN BAKER
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K032357 |
07/30/2003 |
NOVUS TTX LASER AND DELIVERY DEVICES WITH ACCESSORIES |
LUMENIS, INC. |
| K973470 |
09/12/1997 |
COHERENT POPEYE OPHTHALMIC LASER SYSTEM, COHERENT POPEYE OPHTHALMIC LASER SYSTEM IN COMBINATION WITH THE COHERENT ARGONS |
LUMENIS, INC. |
| K004006 |
12/26/2000 |
SELECTA 7000 FREQUENCY DOUBLED, Q-SWITCHED ND:YAG OPHTHALMIC LASER |
LUMENIS, INC. |
| K022181 |
07/03/2002 |
NOVUS VARIA OPHTHALMIC LASER AND DELIVERY DEVICES WITH ACCESSORIES |
LUMENIS, INC. |
| K051944 |
07/18/2005 |
FAMILY OF SELECTA OPHTHALMIC LASER SYSTEMS (SELECTA 1064, SELECTA SLT, SELECTA DUO), DELIVERY DEVICE AND ACCESSORIES |
LUMENIS, INC. |
| K052129 |
08/05/2005 |
LUMENIS 1000 INTEGRATED SLIT LAMP |
LUMENIS, INC. |
| K052526 |
09/14/2005 |
NOVUS 3000 LASER SYSTEM AND DELIVERY DEVICES |
LUMENIS, INC. |
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