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MODIFICATION TO FLOW 7000 PERIPHERAL VASCULAR COIL

Page Type
Cleared 510(K)
510(k) Number
K010730
510(k) Type
Traditional
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/2001
Days to Decision
65 days
Submission Type
Summary

MODIFICATION TO FLOW 7000 PERIPHERAL VASCULAR COIL

Page Type
Cleared 510(K)
510(k) Number
K010730
510(k) Type
Traditional
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/2001
Days to Decision
65 days
Submission Type
Summary