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Escalon Trek Medical
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K963417
VITLITE (TR7700)
December 20, 1996
K963434
VISCOUS FLUID SYSTEM
November 25, 1996
K924999
AUTOPOLE REGULATOR SYSTEM
December 24, 1992