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MODEL 439-07 AND 439-09 LIFELINE MYOCARDIAL LEAD

Page Type
Cleared 510(K)
510(k) Number
K880551
510(k) Type
Traditional
Applicant
INTERMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/1988
Days to Decision
27 days

MODEL 439-07 AND 439-09 LIFELINE MYOCARDIAL LEAD

Page Type
Cleared 510(K)
510(k) Number
K880551
510(k) Type
Traditional
Applicant
INTERMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/1988
Days to Decision
27 days