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KONTRON PMS 7000

Page Type
Cleared 510(K)
510(k) Number
K812354
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/1981
Days to Decision
37 days

KONTRON PMS 7000

Page Type
Cleared 510(K)
510(k) Number
K812354
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/1981
Days to Decision
37 days