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QUANTUM BIPOLAR CARDIAC PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K831633
510(k) Type
Traditional
Applicant
INTERMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/12/1983
Days to Decision
145 days

QUANTUM BIPOLAR CARDIAC PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K831633
510(k) Type
Traditional
Applicant
INTERMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/12/1983
Days to Decision
145 days