ClearanceBrief
Company ยท US

Lkc Technologies, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1976 to 2015. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DRGTransmitters And Receivers, Physiological Signal, Radiofrequency1
GWEStimulator, Photic, Evoked Response1
GWFStimulator, Electrical, Evoked Response1
HITTester, Color Vision1
HIWAnomaloscope1
HLXPhotostimulator, Ac-Powered1
HLZElectrode, Corneal1
HPTPerimeter, Automatic, Ac-Powered1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
May 19, 2015K142567RETeval Visual Electrodiagnostic Device
Lkc Technologies, Inc.
GWE
Oct 25, 1991K914163SCOPTOPIC SENSITIVITY TEST-1[SST-1]
Lkc Technologies, Inc.
HLX
Oct 23, 1991K913962ANOMALOSCOPE QUADRANT TEST-6
Lkc Technologies, Inc.
HIW
Feb 5, 1988K875026ANOMALOSCOPE PLATE TEST - 5 [APT-5]
Lkc Technologies, Inc.
HIT
Jan 12, 1988K874336PATTERN DISCRIMINATION PERIMETER
Lkc Technologies, Inc.
HPT
Mar 4, 1982K820414UNIVERSAL TESTING & ANALYSIS SYSTEMS
Lkc Technologies, Inc.
GWF
Mar 16, 1979K790109TELEMETRY, BIOMEDICAL
Lkc Technologies, Inc.
DRG
Aug 4, 1976K760199ELECTRORETINOGRAPH
Lkc Technologies, Inc.
HLZ

Latest recalls

DateFirm and productCodeLinked 510(k)
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