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Umi, 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
K883527
GRID/RADIOGRAPHIC
September 2, 1988
K831412
CRM-100 COLOR VIDEO CAMERA
June 3, 1983
K830924
CRM-114 COLOR VIDEO CAMERA
April 18, 1983
K823382
NEPHROSTOMY CATHETER
January 28, 1983