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DUAL CHENNEL BRAIN ACTIVITY MONITOR

Page Type
Cleared 510(K)
510(k) Number
K843808
510(k) Type
Traditional
Applicant
DATEX DIVISION INSTRUMENTARIUM CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/1984
Days to Decision
42 days

DUAL CHENNEL BRAIN ACTIVITY MONITOR

Page Type
Cleared 510(K)
510(k) Number
K843808
510(k) Type
Traditional
Applicant
DATEX DIVISION INSTRUMENTARIUM CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/1984
Days to Decision
42 days