Device Classification Name |
Stimulator, Muscle, Powered, For Muscle Conditioning
More FDA Info for this Device |
510(K) Number |
K130723 |
Device Name |
Stimulator, Muscle, Powered, For Muscle Conditioning |
Applicant |
FAMIDOC TECHNOLOGY CO., LTD
No.212 Yilong Road, Hexi Industrial Zone, Jinxia,
Changan Town
Dongguan 523853 CN
Other 510(k) Applications for this Company
|
Contact |
REANNY WANG
Other 510(k) Applications for this Contact |
Regulation Number |
890.5850
More FDA Info for this Regulation Number |
Classification Product Code |
NGX
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
03/18/2013 |
Decision Date |
02/07/2014 |
Decision |
SESE - SUBST EQUIV |
Classification Advisory Committee |
PM - Physical Medicine |
Review Advisory Committee |
PM - Physical Medicine |
Statement / Summary / Purged Status |
Summary |
Type |
Traditional |
Reviewed By Third Party |
N |
Expedited Review |
|