Last synced on 14 November 2025 at 11:06 pm

IMPLANTABLE PROGRAM. CARDIAC PULSE GEN

Page Type
Cleared 510(K)
510(k) Number
K831771
510(k) Type
Traditional
Applicant
TELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/1983
Days to Decision
75 days

IMPLANTABLE PROGRAM. CARDIAC PULSE GEN

Page Type
Cleared 510(K)
510(k) Number
K831771
510(k) Type
Traditional
Applicant
TELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/1983
Days to Decision
75 days