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EMG BIOFEEDBACK DEVICE

Page Type
Cleared 510(K)
510(k) Number
K823511
510(k) Type
Traditional
Applicant
NEMECTRON MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/1983
Days to Decision
122 days

EMG BIOFEEDBACK DEVICE

Page Type
Cleared 510(K)
510(k) Number
K823511
510(k) Type
Traditional
Applicant
NEMECTRON MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/1983
Days to Decision
122 days