Lkc Technologies, Inc. is one of 5098 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lkc Technologies, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Lkc Technologies, Inc. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 8 cleared submissions from 1976 to 2015. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Lkc Technologies, Inc. Filter by specialty or product code using the sidebar.
Lkc Technologies, Inc. — FDA 510(k) Products and Clearance History
8 devices
Cleared
May 19, 2015
RETeval Visual Electrodiagnostic Device
Neurology
249d
Cleared
Oct 25, 1991
SCOPTOPIC SENSITIVITY TEST-1[SST-1]
Ophthalmic
38d
Cleared
Oct 23, 1991
ANOMALOSCOPE QUADRANT TEST-6
Ophthalmic
48d
Cleared
Feb 05, 1988
ANOMALOSCOPE PLATE TEST - 5 [APT-5]
Ophthalmic
60d
Cleared
Jan 12, 1988
PATTERN DISCRIMINATION PERIMETER
Ophthalmic
82d
Cleared
Mar 04, 1982
UNIVERSAL TESTING & ANALYSIS SYSTEMS
Neurology
20d
Cleared
Mar 16, 1979
TELEMETRY, BIOMEDICAL
Cardiovascular
58d
Cleared
Aug 04, 1976
ELECTRORETINOGRAPH
Ophthalmic
28d