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VIVALITH II 301 PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K844334
510(k) Type
Traditional
Applicant
PACESETTER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/1985
Days to Decision
64 days

VIVALITH II 301 PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K844334
510(k) Type
Traditional
Applicant
PACESETTER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/1985
Days to Decision
64 days