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HRK-123 KNEE ARRAY COIL

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050299
510(k) Type
Special
Applicant
Mri Devices Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2005
Days to Decision
17 days
Submission Type
Statement

HRK-123 KNEE ARRAY COIL

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050299
510(k) Type
Special
Applicant
Mri Devices Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2005
Days to Decision
17 days
Submission Type
Statement