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BIOFEEDBACK DEVICE EMG1, EMG ULTRA LOW NOISE OPTI.

Page Type
Cleared 510(K)
510(k) Number
K884852
510(k) Type
Traditional
Applicant
MOE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/2/1989
Days to Decision
76 days

BIOFEEDBACK DEVICE EMG1, EMG ULTRA LOW NOISE OPTI.

Page Type
Cleared 510(K)
510(k) Number
K884852
510(k) Type
Traditional
Applicant
MOE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/2/1989
Days to Decision
76 days