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Promaxo MRI System

Page Type
Cleared 510(K)
510(k) Number
K202518
510(k) Type
Traditional
Applicant
Promaxo, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/2021
Days to Decision
183 days
Submission Type
Summary

Promaxo MRI System

Page Type
Cleared 510(K)
510(k) Number
K202518
510(k) Type
Traditional
Applicant
Promaxo, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/2021
Days to Decision
183 days
Submission Type
Summary