Lkc Technologies, Inc.
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K914163 | SCOPTOPIC SENSITIVITY TEST-1[SST-1] | HLX | 1991-10-25 | View |
| 510(k) | K913962 | ANOMALOSCOPE QUADRANT TEST-6 | HIW | 1991-10-23 | View |
| 510(k) | K875026 | ANOMALOSCOPE PLATE TEST - 5 [APT-5] | HIT | 1988-02-05 | View |
| 510(k) | K874336 | PATTERN DISCRIMINATION PERIMETER | HPT | 1988-01-12 | View |
| 510(k) | K820414 | UNIVERSAL TESTING & ANALYSIS SYSTEMS | GWF | 1982-03-04 | View |
| 510(k) | K790109 | TELEMETRY, BIOMEDICAL | DRG | 1979-03-16 | View |
| 510(k) | K760199 | ELECTRORETINOGRAPH | HLZ | 1976-08-04 | View |
No matching devices.
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