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Leica, 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
K951054
XCEL SLIT LAMP
March 22, 1995
K944022
LENSCHEK
November 17, 1994
K922770
UNISTAT BILIRUBINOMETER MODELS 10310 AND 10311
August 18, 1992