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 13, 2026, FDA's public records list HC Electronics with 10 510(k) clearances. The most recent is a 510(k) clearance dated Mar 4, 1981: STEREO AUDITORY TRAINER (MODEL PM228).
| Date | Record | Source |
|---|---|---|
| Mar 4, 1981 | STEREO AUDITORY TRAINER (MODEL PM228)K810031 · EPF | 510(k) clearances |
| Jan 14, 1981 | POST-AURICULAR HEARING AID (#PE830)K810030 · ESD | 510(k) clearances |
| Feb 26, 1980 | PHONIC EAR, MODEL 841LK800340 · ESD | 510(k) clearances |
| Dec 15, 1978 | HEARING AID, POST-AURICULARK782053 · ESD | 510(k) clearances |
| Jun 22, 1978 | PHONIC EARK780936 · EPF | 510(k) clearances |
| Mar 21, 1978 | PHONIC EARK780363 · ESD | 510(k) clearances |
| Jan 11, 1978 | PHONIC MIRROR HANDIVOCIE MODEL 110K772346 · | 510(k) clearances |
| Jan 11, 1978 | PHONIC MIRROR HANDIVOICE MODEL 120K772347 · | 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
