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MODIFICATION TO MEDRAD SPECTRIS MR INJECTOR

Page Type
Cleared 510(K)
510(k) Number
K011991
510(k) Type
Special
Applicant
MEDRAD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/2001
Days to Decision
56 days
Submission Type
Statement

MODIFICATION TO MEDRAD SPECTRIS MR INJECTOR

Page Type
Cleared 510(K)
510(k) Number
K011991
510(k) Type
Special
Applicant
MEDRAD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/2001
Days to Decision
56 days
Submission Type
Statement