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Promaxo MRI System II

Page Type
Cleared 510(K)
510(k) Number
K232361
510(k) Type
Special
Applicant
Promaxo, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/2023
Days to Decision
29 days
Submission Type
Summary

Promaxo MRI System II

Page Type
Cleared 510(K)
510(k) Number
K232361
510(k) Type
Special
Applicant
Promaxo, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/2023
Days to Decision
29 days
Submission Type
Summary