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 14, 2026, FDA's public records list Hancock Laboratories, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Sep 9, 1980: HANCOCK * OBTURATORS.
| Sep 9, 1980 | HANCOCK * OBTURATORSK801885 · DTI | 510(k) clearances |
| Apr 8, 1980 | MODIFIED CATHETER PACKAGEK800703 · DQO | 510(k) clearances |
| Feb 1, 1980 | HANCOCK AORTIC PUNCHK800122 · DWS | 510(k) clearances |
| Mar 26, 1979 | MERSILENE SUTURESK790534 · KRH | 510(k) clearances |
| May 26, 1978 | DURAN FLEXIBLE RINGK780568 · | 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
