Last synced on 14 November 2025 at 11:06 pm

KONTRON SUPERMON CARDIAC OUTPUT MODULE 7263

Page Type
Cleared 510(K)
510(k) Number
K862261
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/1987
Days to Decision
251 days

KONTRON SUPERMON CARDIAC OUTPUT MODULE 7263

Page Type
Cleared 510(K)
510(k) Number
K862261
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/1987
Days to Decision
251 days