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 Snyder Laboratories, Inc. with 16 510(k) clearances. The most recent is a 510(k) clearance dated Nov 5, 1984: SNYDER HEMOVAC WOUND DRAINAGE DEVICES.
| Nov 5, 1984 | SNYDER HEMOVAC WOUND DRAINAGE DEVICESK843906 · GBS | 510(k) clearances |
| Aug 6, 1982 | SNYDER DEBRIBEMENT SYSTEM LDP-1K821321 · BTA | 510(k) clearances |
| May 2, 1980 | SNYDER HEMOVAC CHEST DRAINAGE SOLUTIONK800861 · KDQ | 510(k) clearances |
| Apr 16, 1980 | SNYDER HEMOVAC TM VENTED WOUND KITK800577 · GCY | 510(k) clearances |
| Apr 16, 1980 | SNYDER HYSTERECTOMY Y TUBE KITK800543 · GCY | 510(k) clearances |
| Apr 16, 1980 | SURGIVAC TMK800578 · GCY | 510(k) clearances |
| Apr 2, 1980 | 100 ML SNYDER HEMOVACK800542 · GCY | 510(k) clearances |
| May 11, 1979 | GREENLINE IRRIGATION TRAYSK790607 · EYN | 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
