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ASTRA T2, T3, T4 & T6 MULTIPROGRAM PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K860585
510(k) Type
Traditional
Applicant
CARDIAC PACEMAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/1986
Days to Decision
148 days

ASTRA T2, T3, T4 & T6 MULTIPROGRAM PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K860585
510(k) Type
Traditional
Applicant
CARDIAC PACEMAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/1986
Days to Decision
148 days