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MODIFIED INTERSEPT PEDIATRIC BLOOD FILTER

Page Type
Cleared 510(K)
510(k) Number
K880671
510(k) Type
Traditional
Applicant
MEDTRONIC BLOOD SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/1988
Days to Decision
78 days

MODIFIED INTERSEPT PEDIATRIC BLOOD FILTER

Page Type
Cleared 510(K)
510(k) Number
K880671
510(k) Type
Traditional
Applicant
MEDTRONIC BLOOD SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/1988
Days to Decision
78 days