Device Classification Name |
Percussor, Powered-Electric
|
510(k) Number |
K103176 |
Device Name |
FREQUENCER |
Applicant |
DYMEDSO INC. |
127 MAIN ST. PO BOX 826 |
SPRINGFIELD,
VT
05156 -0826
|
|
Applicant Contact |
Jean Bigoney |
Correspondent |
DYMEDSO INC. |
127 MAIN ST. PO BOX 826 |
SPRINGFIELD,
VT
05156 -0826
|
|
Correspondent Contact |
Jean Bigoney |
Regulation Number | 868.5665
|
Classification Product Code |
|
Date Received | 10/28/2010 |
Decision Date | 01/26/2011 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Anesthesiology
|
510k Review Panel |
Anesthesiology
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|