ClearanceBrief
Company ยท US

Faxitron Bioptics, LLC

FDA 510(k) clearances and medical device recalls filed under this name, 2012 to 2019. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
MWPCabinet, X-Ray System5

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 14, 2019K183142PathVisionXL
Faxitron Bioptics, LLC
MWP
May 9, 2018K173309Faxitron VisionCT
Faxitron Bioptics, LLC
MWP
Jul 18, 2017K170786Faxitron Bioptics Speciemen Radiography System
Faxitron Bioptics, LLC
MWP
Apr 1, 2016K153583BioVision Plus
Faxitron Bioptics, LLC
MWP
Sep 25, 2012K122428FAXITRON SPECIEN RADIOGRAPHY SYSTEM
Faxitron Bioptics, LLC
MWP

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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