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3.0T 8 CHANNEL NEUROVASCULAR (NV) ARRAY COIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032618
510(k) Type
Special
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/2003
Days to Decision
17 days
Submission Type
Summary

3.0T 8 CHANNEL NEUROVASCULAR (NV) ARRAY COIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032618
510(k) Type
Special
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/2003
Days to Decision
17 days
Submission Type
Summary