DistributorLabelled 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 Popper & Sons with 8 510(k) clearances. The most recent is a 510(k) clearance dated May 20, 1991: HYPODERMIC NEEDLES, SINGLE LUMEN.
| May 20, 1991 | HYPODERMIC NEEDLES, SINGLE LUMENK911397 · FCG | 510(k) clearances |
| Oct 26, 1984 | J -JAMSHIDI TYPE-BONE MARROW BIOPSY/ASPIK843830 · GDM | 510(k) clearances |
| Oct 25, 1984 | ILLINOIS STERNUM/ILIAC ASPIRATION NEEDLEK843690 · GDM | 510(k) clearances |
| Aug 9, 1984 | WESCOTT TYPE BIOPSY NEEDLEK842406 · | 510(k) clearances |
| Jun 5, 1984 | ANTRUM NEEDLE-WOLF TYPEK841300 · | 510(k) clearances |
| Jun 5, 1984 | GARDNER TYPE BONE MARROW NEEDLEK841301 · GAA | 510(k) clearances |
| May 2, 1984 | BIERMAN BIOPSY NEEDLEK841299 · GDM | 510(k) clearances |
| Mar 12, 1984 | WESTERMAN-JENSEN BIOPSY NEEDLEK840168 · FCG | 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
