Device Classification Name |
powered laser surgical instrument
|
510(k) Number |
K220426 |
Device Name |
Fiber Dust PRO |
Applicant |
Quanta System Spa |
Via Acquedotto, 109 |
Samarate,
IT
21017
|
|
Applicant Contact |
Dario Bandiera |
Correspondent |
Quanta System Spa |
Via Acquedotto, 109 |
Samarate,
IT
21017
|
|
Correspondent Contact |
Dario Bandiera |
Regulation Number | 878.4810
|
Classification Product Code |
|
Date Received | 02/14/2022 |
Decision Date | 03/16/2022 |
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
|