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MYOTONE EMG MONITOR

Page Type
Cleared 510(K)
510(k) Number
K772005
510(k) Type
Traditional
Applicant
MICROTRONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/1977
Days to Decision
33 days

MYOTONE EMG MONITOR

Page Type
Cleared 510(K)
510(k) Number
K772005
510(k) Type
Traditional
Applicant
MICROTRONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/1977
Days to Decision
33 days