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MODIFIED MODEL 5330 AV DEMAND PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K910237
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/1991
Days to Decision
38 days

MODIFIED MODEL 5330 AV DEMAND PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K910237
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/1991
Days to Decision
38 days