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Vts, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K012619
VT-1
November 9, 2001
K012662
SE-100 VACUUM ERECTION DEVICE
November 9, 2001
K012639
SE-300 VACUUM THERAPY SYSTEM
November 9, 2001
K012620
SE-200
November 9, 2001
K992442
V.T.S., INC. (V.T.-3)
October 5, 1999