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FDA 510(k) Application Details - K110057
Device Classification Name
Stimulator, Muscle, Powered, For Muscle Conditioning
More FDA Info for this Device
510(K) Number
K110057
Device Name
Stimulator, Muscle, Powered, For Muscle Conditioning
Applicant
MJ SPECIALTY RETAIL
77325 JOYCE WAY
ECHO, OR 97826 US
Other 510(k) Applications for this Company
Contact
CHARLES MACK
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
01/10/2011
Decision Date
10/28/2011
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
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