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Morpheus RealTime Ultrasound, Pathway RealTime Ultrasound, QuickScan Bladder Ultrasound

Page Type
Cleared 510(K)
510(k) Number
K160792
510(k) Type
Traditional
Applicant
THE PROMETHEUS GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/2016
Days to Decision
23 days
Submission Type
Summary

Morpheus RealTime Ultrasound, Pathway RealTime Ultrasound, QuickScan Bladder Ultrasound

Page Type
Cleared 510(K)
510(k) Number
K160792
510(k) Type
Traditional
Applicant
THE PROMETHEUS GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/2016
Days to Decision
23 days
Submission Type
Summary