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 14, 2026, FDA's public records list Randwal Instrument Co. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Feb 5, 1988: IRAS EDS INTERFEROMETRIC STIMULATOR.
| Feb 5, 1988 | IRAS EDS INTERFEROMETRIC STIMULATORK873990 · HLX | 510(k) clearances |
| Nov 24, 1987 | IRAS GLARE TESTERK873987 · HLJ | 510(k) clearances |
| Dec 12, 1986 | IRAS PERIMETERK864012 · HPJ | 510(k) clearances |
| Nov 1, 1985 | LASER IRASK853556 · HPJ | 510(k) clearances |
| Aug 15, 1984 | PORTABLE ACUIOMETERK842567 · HLJ | 510(k) clearances |
| Jan 24, 1983 | VARIABLE CONTRAST ACUIOMETER, DIAGNOSTIC LASER INTERFEROMETERK827577 · | 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
