Last synced on 14 November 2025 at 11:06 pm

GENERATOR, PULSE, MODEL 5997

Page Type
Cleared 510(K)
510(k) Number
K781252
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/1978
Days to Decision
74 days

GENERATOR, PULSE, MODEL 5997

Page Type
Cleared 510(K)
510(k) Number
K781252
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/1978
Days to Decision
74 days