Last synced on 14 November 2025 at 11:06 pm

EMBOL-X AORTIC OCCLUSION AND CARDIOPLEGIA CANNULA

Page Type
Cleared 510(K)
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)
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