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 Output with 5 510(k) clearances. The most recent is a 510(k) clearance dated Feb 29, 1980: OUTPUT DIGITAL DISPLAY MODULE, MOD. 611.
| Date | Record | Source |
|---|---|---|
| Feb 29, 1980 | OUTPUT DIGITAL DISPLAY MODULE, MOD. 611K800360 · DSK | 510(k) clearances |
| Oct 6, 1978 | PRINTER, DIGITALK781115 · DSF | 510(k) clearances |
| May 31, 1978 | OUTPUT DIGITAL DISPLAY MODULE, MODEL 401K780356 · DSK | 510(k) clearances |
| Jun 14, 1977 | NERVE STIMULATOR, MOLEL NO. FB-800K770987 · GZI | 510(k) clearances |
| Nov 19, 1976 | PERIPHERAL NERVE STIMULATORK760614 · BXN | 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
