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ASTRA T2, T3, T4, T6 PULSE GENERATORS NEW PACKAGE

Page Type
Cleared 510(K)
510(k) Number
K890785
510(k) Type
Traditional
Applicant
CARDIAC PACEMAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/1989
Days to Decision
23 days

ASTRA T2, T3, T4, T6 PULSE GENERATORS NEW PACKAGE

Page Type
Cleared 510(K)
510(k) Number
K890785
510(k) Type
Traditional
Applicant
CARDIAC PACEMAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/1989
Days to Decision
23 days