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CARDIAC PACER, MODEL 208

Page Type
Cleared 510(K)
510(k) Number
K780066
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/1978
Days to Decision
18 days

CARDIAC PACER, MODEL 208

Page Type
Cleared 510(K)
510(k) Number
K780066
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/1978
Days to Decision
18 days