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MILLENNIUM 9000 PHASED ARRAY NEUROVASCULAR COIL

Page Type
Cleared 510(K)
510(k) Number
K001870
510(k) Type
Traditional
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2000
Days to Decision
55 days
Submission Type
Summary

MILLENNIUM 9000 PHASED ARRAY NEUROVASCULAR COIL

Page Type
Cleared 510(K)
510(k) Number
K001870
510(k) Type
Traditional
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2000
Days to Decision
55 days
Submission Type
Summary