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Suredrop, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K884974
ACCESSORY TO EYEDROP GUIDE
March 24, 1989
K874569
SUREDROP EYEDROP GUIDE
May 3, 1988