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MYOMETER EMG BIOFEEDBACK DEVICE

Page Type
Cleared 510(K)
510(k) Number
K850849
510(k) Type
Traditional
Applicant
PHYSIO TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/1985
Days to Decision
91 days

MYOMETER EMG BIOFEEDBACK DEVICE

Page Type
Cleared 510(K)
510(k) Number
K850849
510(k) Type
Traditional
Applicant
PHYSIO TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/1985
Days to Decision
91 days