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VASCULAR ARCHITECTS PERISCOPE DEVICE

Page Type
Cleared 510(K)
510(k) Number
K003719
510(k) Type
Traditional
Applicant
Vascular Architects, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2001
Days to Decision
86 days
Submission Type
Summary

VASCULAR ARCHITECTS PERISCOPE DEVICE

Page Type
Cleared 510(K)
510(k) Number
K003719
510(k) Type
Traditional
Applicant
Vascular Architects, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2001
Days to Decision
86 days
Submission Type
Summary