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MODIFICATION TO MEDRAD SPECTRIS MR INJECTOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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