Last synced on 25 January 2026 at 3:41 am

HRK-63-8 KNEE ARRAY COIL

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032633
510(k) Type
Special
Applicant
Mri Devices Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/2003
Days to Decision
30 days
Submission Type
Statement

HRK-63-8 KNEE ARRAY COIL

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032633
510(k) Type
Special
Applicant
Mri Devices Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/2003
Days to Decision
30 days
Submission Type
Statement