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Alcon Surgical, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K902798
AUTOMATED HYDROSONICS(TM)
August 28, 1990
K901275
RETINAL TAAK
March 23, 1990
K897099
MODEL 2800 ND:YAG OPHTHALMIC LASER
February 16, 1990