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AFP PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K823559
510(k) Type
Traditional
Applicant
PACESETTER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/18/1983
Days to Decision
78 days

AFP PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K823559
510(k) Type
Traditional
Applicant
PACESETTER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/18/1983
Days to Decision
78 days