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Cannon U.S.A., 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
K960839
FILM SCANNER 300
December 18, 1996
K942242
AUTO REF-KERATOMETER, RK-3
September 2, 1994