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Sheaumann Laser, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
2
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K150664
NeoLas
December 22, 2015
K120938
THE PL-1064 LASER SYSTEM
September 24, 2012