Biotech companyLabelled 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., part of BayerLabelled 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. See the Bayer group view.
As of Nov 14, 2026, FDA's public records list Cutter Laboratories with 39 510(k) clearances. The most recent is a 510(k) clearance dated May 21, 1986: HYPERBARIC PENETRATION EXTENSION SET.
| May 21, 1986 | HYPERBARIC PENETRATION EXTENSION SETK861315 · CBF | 510(k) clearances |
| Mar 17, 1986 | BAYSILEXK854106 · ELW | 510(k) clearances |
| Nov 9, 1984 | PERFOURMK842324 · ELW | 510(k) clearances |
| May 30, 1984 | INTRAVENOUS INFUSION CONTROLLERK834106 · LDR | 510(k) clearances |
| Aug 16, 1983 | ORTHOPEDIC CASTING TAPE MAXCASTK832237 · ITG | 510(k) clearances |
| Jan 12, 1983 | DOSIMETRIC RELEASE PROGRAM - ADMIN. SETK823214 · FPA | 510(k) clearances |
| May 28, 1982 | CUTTER BOND POLYCARBOXYLATE CEMENTK821326 · EMA | 510(k) clearances |
| Mar 2, 1982 | CUTTERBOND ZINC PHOSPHATE CEMENTK813532 · EMA | 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
