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CTL-63-8 CERVICAL/THORACIC/LUMBAR SPINE ARRAY COIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022720
510(k) Type
Special
Applicant
MRI DEVICES CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/2002
Days to Decision
22 days
Submission Type
Statement

CTL-63-8 CERVICAL/THORACIC/LUMBAR SPINE ARRAY COIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022720
510(k) Type
Special
Applicant
MRI DEVICES CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/2002
Days to Decision
22 days
Submission Type
Statement