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Acueity, Inc.

FDA Regulatory Profile

Acueity, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 7, 2004.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K040949VIADUCT MINISCOPE AND ACCESSORIESMay 7, 2004
K032847EXCISOR BIOPTOME, MODEL 01-0004September 26, 2003
K032430ACUEITY MEDICAL LIGHT SOURCESeptember 5, 2003
K011189VIADUCT MICROENDOSCOPE AND ACCESSORIESJuly 16, 2001

FDA data resources