Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Amplaid USA with 8 510(k) clearances. The most recent is a 510(k) clearance dated Aug 20, 1986: AMPLAID MK15 (EVOKED POTENTIAL SYSTEM).
| Aug 20, 1986 | AMPLAID MK15 (EVOKED POTENTIAL SYSTEM)K861014 · GWL | 510(k) clearances |
| Nov 25, 1983 | EVOKED POTENTIALS SYSTEM MK10K832510 · GWJ | 510(k) clearances |
| Apr 29, 1981 | SOMATOSENSORY STIMULATORK810482 · GWF | 510(k) clearances |
| Apr 29, 1981 | MK6 ERA SYSTEMK810473 · GWJ | 510(k) clearances |
| Mar 11, 1981 | VISUAL PATTERN REVERSAL GEN. & PHOTIC S.K810481 · GWE | 510(k) clearances |
| Dec 19, 1980 | 101, 151, 161 PORTABLE AUDIOMETERSK802963 · EWO | 510(k) clearances |
| Oct 10, 1980 | SELF-RECORDING ADMITTANCE METER 709K802097 · ETY | 510(k) clearances |
| Nov 3, 1978 | AMPLAID MARK 4 AND MARK 5K781667 · GWJ | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
