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3.0T 8-CHANNEL CTL SPINE ARRAY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K042186
510(k) Type
Special
Applicant
Usa Instruments, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/26/2004
Days to Decision
14 days
Submission Type
Summary

3.0T 8-CHANNEL CTL SPINE ARRAY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K042186
510(k) Type
Special
Applicant
Usa Instruments, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/26/2004
Days to Decision
14 days
Submission Type
Summary