Medical Vision Ab

FDA Regulatory Profile

Summary

Total Recalls
1
510(k) Clearances
1
Inspections
1
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-2705-2016Class IIDouble Pump RF Patient Cassette; Product Number: 72204055. Intended to provide fluid distension aMay 10, 2016

Recent 510(k) Clearances

K-NumberDeviceDate
K093409POWERPUMP ARTHROSCOPY SYSTEMFebruary 24, 2010