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 H.W. Andersen Products, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Dec 30, 1994: AN-10S ANDERSEN TUBE WITH STYLET.
| Dec 30, 1994 | AN-10S ANDERSEN TUBE WITH STYLETK935688 · BSS | 510(k) clearances |
| Sep 21, 1987 | AN3200 DOUBILET DRAINK872458 · FGE | 510(k) clearances |
| Jul 23, 1987 | AN3000 MAHONEY DRAINK872460 · GBS | 510(k) clearances |
| Jul 21, 1987 | AN3500 WORTH DRAINK872457 · GBS | 510(k) clearances |
| Jul 21, 1987 | AN3100 MULHOLLAND DRAINK872459 · GBS | 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
