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MRIDIUM 3850 MRI PUMP SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K050301
510(k) Type
Traditional
Applicant
IRADIMED CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/2005
Days to Decision
44 days
Submission Type
Summary

MRIDIUM 3850 MRI PUMP SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K050301
510(k) Type
Traditional
Applicant
IRADIMED CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/2005
Days to Decision
44 days
Submission Type
Summary