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Moti Enterprises, 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
K843437
MEI MAMMOGRAPHY SYS MX-2049
November 27, 1984
K810095
MOTI APRON
February 12, 1981
K802377
MOTI PROTECTIVE X-RAY MASK
October 31, 1980