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CARDIOPULMINARY BYPASS CATHETER CANNULA

Page Type
Cleared 510(K)
510(k) Number
K810548
510(k) Type
Traditional
Applicant
DLP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/17/1981
Days to Decision
15 days

CARDIOPULMINARY BYPASS CATHETER CANNULA

Page Type
Cleared 510(K)
510(k) Number
K810548
510(k) Type
Traditional
Applicant
DLP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/17/1981
Days to Decision
15 days