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GENERATOR, PULSE, DEMAND, MODEL 5996

Page Type
Cleared 510(K)
510(k) Number
K780741
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/1978
Days to Decision
88 days

GENERATOR, PULSE, DEMAND, MODEL 5996

Page Type
Cleared 510(K)
510(k) Number
K780741
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/1978
Days to Decision
88 days