Device Classification Name |
powered laser surgical instrument
|
510(k) Number |
K010284 |
Device Name |
LYRA G SERIES SURGICAL LASER SYSTEM (SL SERIES Q-SWITCHED ND:YAG CONFIGURATION) |
Applicant |
LASERSCOPE |
3070 ORCHARD DR. |
SAN JOSE,
CA
95134 -2011
|
|
Applicant Contact |
PAUL H HARDIMAN |
Correspondent |
LASERSCOPE |
3070 ORCHARD DR. |
SAN JOSE,
CA
95134 -2011
|
|
Correspondent Contact |
PAUL H HARDIMAN |
Regulation Number | 878.4810
|
Classification Product Code |
|
Date Received | 01/31/2001 |
Decision Date | 05/01/2001 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General & Plastic Surgery
|
510k Review Panel |
General & Plastic Surgery
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
Recalls |
CDRH Recalls
|