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ASTRA T2, ASTRA T4, ASTRA T6

Page Type
Cleared 510(K)
510(k) Number
K920601
510(k) Type
Traditional
Applicant
CARDIAC PACEMAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/1992
Days to Decision
260 days
Submission Type
Summary

ASTRA T2, ASTRA T4, ASTRA T6

Page Type
Cleared 510(K)
510(k) Number
K920601
510(k) Type
Traditional
Applicant
CARDIAC PACEMAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/1992
Days to Decision
260 days
Submission Type
Summary