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MODEL 221 PROGRAMALITH PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K790873
510(k) Type
Traditional
Applicant
PACESETTER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/20/1979
Days to Decision
136 days

MODEL 221 PROGRAMALITH PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K790873
510(k) Type
Traditional
Applicant
PACESETTER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/20/1979
Days to Decision
136 days