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 15, 2026, FDA's public records list Shaban Mfg. Co. with 35 510(k) clearances. The most recent is a 510(k) clearance dated Dec 5, 1985: REPLACEMENT PUMP TUBING.
| Dec 5, 1985 | REPLACEMENT PUMP TUBINGK853621 · JJE | 510(k) clearances |
| Feb 27, 1985 | CANNULAS FOR HEMA-TEK I & KK SLIDE STAINERSK850157 · KPA | 510(k) clearances |
| Feb 27, 1985 | PUMP TUBE SETS FOR HEMA-TEK I & II SLIDE STAINERSK850333 · KPA | 510(k) clearances |
| Feb 1, 1985 | MEMBRANE KITS-KC1, CO2 & 02 FOR INSTRUMENT-LABK844781 · CHL | 510(k) clearances |
| Nov 20, 1984 | CHLORIDE STANDARDK844235 · JIS | 510(k) clearances |
| Aug 12, 1984 | REPLACEMENT PARTS NOVA ELECTROLYTE ANALK842656 · JFL | 510(k) clearances |
| May 25, 1984 | COMPONENTS FOR PARTIAL PRESSURE ELEEK841609 · CHL | 510(k) clearances |
| May 25, 1984 | COMPONENTS FOR POTASSIUM, SODIUM CHLOK841610 · JGT | 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
