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MRI PATIENT POSITIONING DEVICES

Page Type
Cleared 510(K)
510(k) Number
K093738
510(k) Type
Traditional
Applicant
MEDTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/2010
Days to Decision
161 days
Submission Type
Summary

MRI PATIENT POSITIONING DEVICES

Page Type
Cleared 510(K)
510(k) Number
K093738
510(k) Type
Traditional
Applicant
MEDTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/2010
Days to Decision
161 days
Submission Type
Summary