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INTERVENTIONAL PRODUCTS - GUIDE WIRES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890207
510(k) Type
Traditional
Applicant
E-Z-EM, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/1989
Days to Decision
134 days

INTERVENTIONAL PRODUCTS - GUIDE WIRES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890207
510(k) Type
Traditional
Applicant
E-Z-EM, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/1989
Days to Decision
134 days