Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Positron Corp. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jul 12, 2002: MPOWER, MODEL 712 SERIES.
| Date | Record | Source |
|---|---|---|
| Jul 12, 2002 | MPOWER, MODEL 712 SERIESK022001 · KPS | 510(k) clearances |
| Jul 8, 1993 | POSICAM-HZ & POSICAM-HZLK926206 · KPS | 510(k) clearances |
| May 9, 1991 | POSICAM SYSTEM MODEL 6.5 POSICAM-HZ SYSTEMK911275 · KPS | 510(k) clearances |
| Nov 2, 1989 | MODIFIED POSICAM SYSTEM MODEL 6.5K894998 · KPS | 510(k) clearances |
| Mar 11, 1981 | AUTOMATIC SCREENING AUDIOMETERK810537 · EWO | 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
