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LEO III TX/RX QUADRATURE KNEE COIL; ALPHA III TX/RX QUADRATURE WRIST COIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023982
510(k) Type
Traditional
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/2003
Days to Decision
81 days
Submission Type
Summary

LEO III TX/RX QUADRATURE KNEE COIL; ALPHA III TX/RX QUADRATURE WRIST COIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023982
510(k) Type
Traditional
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/2003
Days to Decision
81 days
Submission Type
Summary