Device Classification Name |
powered laser surgical instrument
|
510(k) Number |
K060338 |
Device Name |
FAMILY OF SELECTA LASER SYSTEMS INCLUDING SELECTA 1064, SELECTA SLT, SELECTA DUET, SELECTA DUO, SELECTA TRIO |
Applicant |
LUMENIS, INC. |
2400 CONDENSA ST. |
SANTA CLARA,
CA
95051 -0901
|
|
Applicant Contact |
Connie Hoy |
Correspondent |
LUMENIS, INC. |
2400 CONDENSA ST. |
SANTA CLARA,
CA
95051 -0901
|
|
Correspondent Contact |
Connie Hoy |
Regulation Number | 878.4810
|
Classification Product Code |
|
Date Received | 02/10/2006 |
Decision Date | 03/09/2006 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General & Plastic Surgery
|
510k Review Panel |
General & Plastic Surgery
|
Summary |
Summary
|
Type |
Special
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|