Last synced on 30 September 2022 at 11:05 pm

DUAL CHENNEL BRAIN ACTIVITY MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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