LKC Technologies, Inc.
Germantown, MD, US
LKC TECHNOLOGIES, INC. appears in FDA device records in Germantown, MD. FDA records list 8 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 8 510(k) clearances for LKC Technologies, Inc. between 1976 and 2015. The busiest year on record is 1988, with 2. The most recent is 2015, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1976 | 1 |
| 1979 | 1 |
| 1982 | 1 |
| 1988 | 2 |
| 1991 | 2 |
| 2015 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K142567 | RETeval Visual Electrodiagnostic Device | GWE | Substantially Equivalent | |
| K914163 | SCOPTOPIC SENSITIVITY TEST-1[SST-1] | HLX | Substantially Equivalent | |
| K913962 | ANOMALOSCOPE QUADRANT TEST-6 | HIW | Substantially Equivalent | |
| K875026 | ANOMALOSCOPE PLATE TEST - 5 [APT-5] | HIT | Substantially Equivalent | |
| K874336 | PATTERN DISCRIMINATION PERIMETER | HPT | Substantially Equivalent | |
| K820414 | UNIVERSAL TESTING & ANALYSIS SYSTEMS | GWF | Substantially Equivalent | |
| K790109 | TELEMETRY, BIOMEDICAL | DRG | Substantially Equivalent | |
| K760199 | ELECTRORETINOGRAPH | HLZ | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 1119189 | 1119189 | LKC TECHNOLOGIES, INC. | 20501 Seneca Meadows Pkwy Ste 305, Germantown, MD 20876 US | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain