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Zephyr Vascular Compression Device

Page Type
Cleared 510(K)
510(k) Number
K151363
510(k) Type
Traditional
Applicant
ADVANCED VASCULAR DYNAMICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2015
Days to Decision
71 days
Submission Type
Summary

Zephyr Vascular Compression Device

Page Type
Cleared 510(K)
510(k) Number
K151363
510(k) Type
Traditional
Applicant
ADVANCED VASCULAR DYNAMICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2015
Days to Decision
71 days
Submission Type
Summary