Lkc Technologies, Inc.
Lkc Technologies, Inc. holds FDA 510(k) medical device clearances, first cleared 1976, most recent 2015.
Top product codes for Lkc Technologies, Inc.
Recent clearances by Lkc Technologies, Inc.
- K142567 — RETeval Visual Electrodiagnostic Device
- K914163 — SCOPTOPIC SENSITIVITY TEST-1[SST-1]
- K913962 — ANOMALOSCOPE QUADRANT TEST-6
- K875026 — ANOMALOSCOPE PLATE TEST - 5 [APT-5]
- K874336 — PATTERN DISCRIMINATION PERIMETER
- K820414 — UNIVERSAL TESTING & ANALYSIS SYSTEMS
- K790109 — TELEMETRY, BIOMEDICAL
- K760199 — ELECTRORETINOGRAPH
Data sourced from openFDA. This site is unofficial and independent of the FDA.