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PULSE GENERATORS, MODELS 5972/5973

Page Type
Cleared 510(K)
510(k) Number
K780061
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/1978
Days to Decision
13 days

PULSE GENERATORS, MODELS 5972/5973

Page Type
Cleared 510(K)
510(k) Number
K780061
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/1978
Days to Decision
13 days