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Minilap Technologies
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K132232
MINS NEEDLESCOPIC RESPOSABLE DEVICE SYSTEM
December 4, 2013
K113597
MINI-LAP BIPOLAR ELECTROCAUTERY DEVICES
June 3, 2012