Last synced on 14 November 2025 at 11:06 pm

GENERATOR, CARDIAC PULSE, 250B

Page Type
Cleared 510(K)
510(k) Number
K781090
510(k) Type
Traditional
Applicant
TELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/7/1978
Days to Decision
66 days

GENERATOR, CARDIAC PULSE, 250B

Page Type
Cleared 510(K)
510(k) Number
K781090
510(k) Type
Traditional
Applicant
TELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/7/1978
Days to Decision
66 days