Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of GSK. FDA records under its name, each linked to the record. See the GSK group view.
As of Nov 13, 2026, FDA's public records list Geometric Data (SmithKline division) with 18 510(k) clearances. The most recent is a 510(k) clearance dated Sep 5, 1984: AUTOLYZER 800.
| Date | Record | Source |
|---|---|---|
| Sep 5, 1984 | AUTOLYZER 800K841852 · GKZ | 510(k) clearances |
| Aug 18, 1981 | HEMASPINNERK811534 · GKJ | 510(k) clearances |
| Sep 4, 1979 | HEMATRAK ABNORMAL RECOGNITIONK791041 · GKZ | 510(k) clearances |
| Jul 17, 1979 | CONTEXT FILTERK791108 · GKZ | 510(k) clearances |
| Jul 17, 1979 | HEMATRAK MODEL 480K790816 · GKZ | 510(k) clearances |
| Feb 15, 1979 | STAIN, HEMASTAIN RETICK790042 · GJH | 510(k) clearances |
| May 19, 1978 | PLATELETS/CU MMK780577 · GKZ | 510(k) clearances |
| Jan 5, 1978 | RE-CELL SLIDE RECAPK772139 · JOY | 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
