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Luneau SA

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K162067VX130 Ophthalmic Diagnostic DeviceApril 24, 2017
K143086VX120 Ophthalmic Diagnostic DeviceJune 1, 2015
K023838LUNEAU STERILE TONOMETER SEPARATION PRISMSFebruary 20, 2003
K022413LUNEAU 3 MIRROR LENSSeptember 24, 2002
K851557ANESTHESIOMETERMay 30, 1985