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EMBOL-X AORTIC OCCLUSION AND CARDIOPLEGIA CANNULA

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980631
510(k) Type
Traditional
Applicant
Embol-X, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/2/1999
Days to Decision
349 days
Submission Type
Summary

EMBOL-X AORTIC OCCLUSION AND CARDIOPLEGIA CANNULA

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980631
510(k) Type
Traditional
Applicant
Embol-X, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/2/1999
Days to Decision
349 days
Submission Type
Summary