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 Arbrook Mfg. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Oct 26, 1979: DISCARD-A-PAD 40-COUNT SHARPS DISPOSAL.
| Oct 26, 1979 | DISCARD-A-PAD 40-COUNT SHARPS DISPOSALK792016 · MMK | 510(k) clearances |
| Nov 3, 1978 | LATEX, IN-HOUSE COMPOUNDEDK781847 · KGO | 510(k) clearances |
| Aug 31, 1978 | GLOVES, PROCEDUREK781278 · FMC | 510(k) clearances |
| Feb 25, 1977 | GLOVES, SURGEONS,MICRO-TOUCH POWDERFREEK770056 · KGO | 510(k) clearances |
| Aug 23, 1976 | THERMOMETER, SURVALENT-ELECTRONICK760421 · FLL | 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
