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Voss Medical Products
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
5
Inspections
2
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K932186
BYPASS LEG POSITIONER
June 1, 1993
K932187
PRONE POSITIONER
June 1, 1993
K896338
VOSS DISPOSABLE CORONARY BYPASS FLUSHING CANNULA
May 17, 1990
K885161
VOSS VEIN CLAMP
December 22, 1989
K895369
VOSS GRAFT MARKER
September 27, 1989