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Vismed, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K930937
LD 400
October 18, 1993
K873122
TKS 4000 AUTO PERIMETER
November 2, 1987