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CROSSEAL APPLICATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K030032
510(k) Type
Traditional
Applicant
OMRIX BIOPHARMACEUTICALS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2003
Days to Decision
77 days
Submission Type
Summary

CROSSEAL APPLICATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K030032
510(k) Type
Traditional
Applicant
OMRIX BIOPHARMACEUTICALS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2003
Days to Decision
77 days
Submission Type
Summary