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REDINOV PERFUSION SET

Page Type
Cleared 510(K)
510(k) Number
K924010
510(k) Type
Traditional
Applicant
BIPRESS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/1994
Days to Decision
735 days
Submission Type
Statement

REDINOV PERFUSION SET

Page Type
Cleared 510(K)
510(k) Number
K924010
510(k) Type
Traditional
Applicant
BIPRESS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/1994
Days to Decision
735 days
Submission Type
Statement