Last synced on 14 November 2025 at 11:06 pm

INTERSEPT*CRYSTALLOID CARDIOPLEGIA DELIVERY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K883439
510(k) Type
Traditional
Applicant
MEDTRONIC BLOOD SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/13/1988
Days to Decision
59 days

INTERSEPT*CRYSTALLOID CARDIOPLEGIA DELIVERY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K883439
510(k) Type
Traditional
Applicant
MEDTRONIC BLOOD SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/13/1988
Days to Decision
59 days