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AFP MODEL 262T PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K884733
510(k) Type
Traditional
Applicant
PACESETTER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1989
Days to Decision
92 days

AFP MODEL 262T PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K884733
510(k) Type
Traditional
Applicant
PACESETTER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1989
Days to Decision
92 days