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AUTOTRANSFUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K892819
510(k) Type
Traditional
Applicant
IMPRA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/1989
Days to Decision
35 days

AUTOTRANSFUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K892819
510(k) Type
Traditional
Applicant
IMPRA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/1989
Days to Decision
35 days