Lkc Technologies, Inc. is one of 13055 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
Recent clearances: RETeval Visual Electrodiagnostic Device
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.
510(k) submissions have been managed by Regulatory Affairs Associates, Inc. as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Lkc Technologies, Inc.
8 devices
Cleared
CT
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