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PROGRAMALITH III-3 MODEL 231 PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K850651
510(k) Type
Traditional
Applicant
PACESETTER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/1985
Days to Decision
41 days

PROGRAMALITH III-3 MODEL 231 PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K850651
510(k) Type
Traditional
Applicant
PACESETTER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/1985
Days to Decision
41 days