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All-Pro Imaging Corp.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K001314
MEDSCOPE
July 25, 2000
K001321
ALL-PRO 2010
May 16, 2000
K991435
AII-PRO 100 PLUS AND ALL-PRO 200
May 20, 1999
K911291
ALL-PRO 100
July 3, 1991