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MYOTRACE 10 BIOFEEDBACK DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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