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Bioview , Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K130775DUET SYSTEMMay 9, 2014
K061602DUET SYSTEMJanuary 23, 2007
K050840MODIFICATION TO DUET SYSTEMAugust 16, 2005
K040591DUET SYSTEMSeptember 16, 2004
K030192DUET SYSTEMAugust 20, 2003