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PROGRAMMABLE BIPOLAR CARDIAC GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K800837
510(k) Type
Traditional
Applicant
ARCO MEDICAL PRODUCTS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/1980
Days to Decision
76 days

PROGRAMMABLE BIPOLAR CARDIAC GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K800837
510(k) Type
Traditional
Applicant
ARCO MEDICAL PRODUCTS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/1980
Days to Decision
76 days