Last synced on 19 July 2024 at 11:05 pm

VISION 9000 PHASED ARRAY TORSO COIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002482
510(k) Type
Traditional
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/2000
Days to Decision
64 days
Submission Type
Summary

VISION 9000 PHASED ARRAY TORSO COIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002482
510(k) Type
Traditional
Applicant
USA INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/2000
Days to Decision
64 days
Submission Type
Summary