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PULSE GENERATORS, MODELS 5983, 5989

Page Type
Cleared 510(K)
510(k) Number
K790068
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/1979
Days to Decision
259 days

PULSE GENERATORS, MODELS 5983, 5989

Page Type
Cleared 510(K)
510(k) Number
K790068
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/1979
Days to Decision
259 days