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TREMOR MONITOR

Page Type
Cleared 510(K)
510(k) Number
K782036
510(k) Type
Traditional
Applicant
COLUMBUS INSTRUMENTS INTL. CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/1979
Days to Decision
49 days

TREMOR MONITOR

Page Type
Cleared 510(K)
510(k) Number
K782036
510(k) Type
Traditional
Applicant
COLUMBUS INSTRUMENTS INTL. CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/1979
Days to Decision
49 days