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Allergan Humphrey
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K902582
ALLERGAN HUMPHREY A/B SCAN , MODEL 835
August 14, 1990
K872312
MODEL 3000 OPHTHALMIC SURGICAL SYSTEM
July 15, 1987
K871611
ALLERGAN HUMPHREY AUTO-REFRACTOR, MODELS 525 & 540
May 18, 1987