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MYOTRACE 10 BIOFEEDBACK DEVICE

Page Type
Cleared 510(K)
510(k) Number
K895633
510(k) Type
Traditional
Applicant
NORAXON USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/1990
Days to Decision
206 days

MYOTRACE 10 BIOFEEDBACK DEVICE

Page Type
Cleared 510(K)
510(k) Number
K895633
510(k) Type
Traditional
Applicant
NORAXON USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/1990
Days to Decision
206 days