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EXTERNAL TEST PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K780717
510(k) Type
Traditional
Applicant
VITATRON MEDICAL BV
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/1978
Days to Decision
64 days

EXTERNAL TEST PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K780717
510(k) Type
Traditional
Applicant
VITATRON MEDICAL BV
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/1978
Days to Decision
64 days