Last synced on 14 November 2025 at 11:06 pm

COMMAND P5(BIPOLAR PULSE GENERATOR)

Page Type
Cleared 510(K)
510(k) Number
K811402
510(k) Type
Traditional
Applicant
CARDIAC PACEMAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/27/1981
Days to Decision
70 days

COMMAND P5(BIPOLAR PULSE GENERATOR)

Page Type
Cleared 510(K)
510(k) Number
K811402
510(k) Type
Traditional
Applicant
CARDIAC PACEMAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/27/1981
Days to Decision
70 days