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Acueity, 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
K040949
VIADUCT MINISCOPE AND ACCESSORIES
May 7, 2004
K032847
EXCISOR BIOPTOME, MODEL 01-0004
September 26, 2003
K032430
ACUEITY MEDICAL LIGHT SOURCE
September 5, 2003
K011189
VIADUCT MICROENDOSCOPE AND ACCESSORIES
July 16, 2001