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KONTRON E.E.G. MONITOR, SUPERMON MODULE 7265

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K870815
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/1988
Days to Decision
335 days

KONTRON E.E.G. MONITOR, SUPERMON MODULE 7265

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K870815
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/1988
Days to Decision
335 days