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DIGITAL EMG MONITOR MYOTRON 120

Page Type
Cleared 510(K)
510(k) Number
K882266
510(k) Type
Traditional
Applicant
ATS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/1988
Days to Decision
76 days

DIGITAL EMG MONITOR MYOTRON 120

Page Type
Cleared 510(K)
510(k) Number
K882266
510(k) Type
Traditional
Applicant
ATS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/1988
Days to Decision
76 days