Device Classification Name |
electrosurgical, cutting & coagulation & accessories
|
510(k) Number |
K102698 |
Device Name |
PELLEVE GLIDESAFE NON-ABLATIVE WRINKLE TREATMENT SYSTEM MODEL PELLEVE GLIDESAFE |
Applicant |
ELLMAN INT'L INC. |
3333 ROYAL AVENUE |
OCEANSIDE,
NY
11572 -3625
|
|
Applicant Contact |
JONATHAN ACHENBACH |
Correspondent |
ELLMAN INT'L INC. |
3333 ROYAL AVENUE |
OCEANSIDE,
NY
11572 -3625
|
|
Correspondent Contact |
JONATHAN ACHENBACH |
Regulation Number | 878.4400
|
Classification Product Code |
|
Date Received | 09/20/2010 |
Decision Date | 01/05/2011 |
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
|