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EVICEL APPLICATION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130900
510(k) Type
Traditional
Applicant
ETHICON INC (ON BEHALF OF OMRIX BIOPHARACEUTICALS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/2013
Days to Decision
134 days
Submission Type
Summary

EVICEL APPLICATION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130900
510(k) Type
Traditional
Applicant
ETHICON INC (ON BEHALF OF OMRIX BIOPHARACEUTICALS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/2013
Days to Decision
134 days
Submission Type
Summary