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PERIPHERAL VASCULAR DILATOR

Page Type
Cleared 510(K)
510(k) Number
K974617
510(k) Type
Traditional
Applicant
ENDOVASCULAR INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/1998
Days to Decision
355 days
Submission Type
Summary

PERIPHERAL VASCULAR DILATOR

Page Type
Cleared 510(K)
510(k) Number
K974617
510(k) Type
Traditional
Applicant
ENDOVASCULAR INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/1998
Days to Decision
355 days
Submission Type
Summary