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Faxitron Bioptics, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K183142PathVisionXLMarch 14, 2019
K173309Faxitron VisionCTMay 9, 2018
K170786Faxitron Bioptics Speciemen Radiography SystemJuly 18, 2017
K153583BioVision PlusApril 1, 2016
K122428FAXITRON SPECIEN RADIOGRAPHY SYSTEMSeptember 25, 2012