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A.R.C Laser GmbH

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K220531FOX 810, FOX 980September 1, 2022
K192272Wolf445nmMarch 17, 2020
K170183Cetus system, Cetus probeSeptember 27, 2017
K161403A.R.C. Laser Surgical Fibers and ProbesAugust 16, 2016
K091059FOXQ 980 LASERAugust 13, 2009
K073322FOX 1-980, FOX Q-1064, FOX-Q-810February 22, 2008