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ADAPTATION OF KANTRON 40 CC. PDLIAB

Page Type
Cleared 510(K)
510(k) Number
K820166
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/1982
Days to Decision
98 days

ADAPTATION OF KANTRON 40 CC. PDLIAB

Page Type
Cleared 510(K)
510(k) Number
K820166
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/1982
Days to Decision
98 days