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 Pollak (Intl.), Ltd. with 31 510(k) clearances. The most recent is a 510(k) clearance dated Apr 27, 2000: UMBICUT.
| Date | Record | Source |
|---|---|---|
| Apr 27, 2000 | UMBICUTK000227 · HFW | 510(k) clearances |
| Apr 21, 1981 | PEDICAT*K810049 · KMJ | 510(k) clearances |
| Mar 26, 1981 | VECAFIX*K810050 · KGX | 510(k) clearances |
| Oct 31, 1980 | INFUSSION ALARM SYSTEM I.A.S. CAT.#1118K802011 · FLN | 510(k) clearances |
| Oct 31, 1980 | FLOWCLAMP CAT.#1011 & 1012K802009 · FKK | 510(k) clearances |
| Oct 10, 1980 | DRESSING CHANGE SET CAT.#910-930K802017 · KDD | 510(k) clearances |
| Sep 26, 1980 | PEDIWET=GUAZE IMPREGNATED WITH PETROLK802007 · FRQ | 510(k) clearances |
| Sep 16, 1980 | EYE APPLICATORS CAT.#980-983K802016 · KXF | 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
