FirmLabelled 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 its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Gorman-Rupp Industries with 6 510(k) clearances. The most recent is a 510(k) clearance dated Sep 6, 1977: AQUAMATIC K-MODULE MODEL K-20.
| Sep 6, 1977 | AQUAMATIC K-MODULE MODEL K-20K771537 · DWJ | 510(k) clearances |
| Jun 8, 1977 | AQUAMATIC K-77K770839 · DWJ | 510(k) clearances |
| Feb 14, 1977 | BLOOD/FLUID WARMER MODEL DW-1000AK770232 · BSB | 510(k) clearances |
| Jan 10, 1977 | AQUAMATIC K-MODULE MODEL K-10K761337 · JRR | 510(k) clearances |
| Dec 16, 1976 | DISPOSABLE K-PADSK760910 · ILO | 510(k) clearances |
| Dec 6, 1976 | ELECTRONIC CONTROL UNITK761087 · DWJ | 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
