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Expanded Optics, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K922321
OMNI ARTHROSCOPE
August 3, 1993
K922319
OMNI LAPAROSCOPE
April 23, 1993
K922320
OMNI CYSTOSCOPE
January 13, 1993
K894570
UNIVERSAL LIGHT CABLE
October 13, 1989