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MODEL #QWH-63, QUADRATURE WRIST AND HAND COIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931008
510(k) Type
Traditional
Applicant
MRI DEVICES CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/1993
Days to Decision
112 days
Submission Type
Statement