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 Lab Ability with 5 510(k) clearances. The most recent is a 510(k) clearance dated Dec 30, 1983: SELECTO-DISC NOVOBIOCIN 5UG.
| Date | Record | Source |
|---|---|---|
| Dec 30, 1983 | SELECTO-DISC NOVOBIOCIN 5UGK833407 · JTO | 510(k) clearances |
| Sep 26, 1983 | SELECTRO-DISCK832436 · JTO | 510(k) clearances |
| Feb 9, 1983 | Q-CHECK CULTI-LOOPSK830133 · JTR | 510(k) clearances |
| Jan 9, 1983 | Q-CHECK REAGENT STANDARDSK830134 · LJG | 510(k) clearances |
| Dec 3, 1981 | SHIGELLA SERA-CHEKK813191 · LIA | 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
