Diagnostics 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 Diag Corp. with 9 510(k) clearances. The most recent is a 510(k) clearance dated Mar 24, 1999: SEAL-AWAY HEMOSTASIS ADAPTER, MODEL 406229.
| Mar 24, 1999 | SEAL-AWAY HEMOSTASIS ADAPTER, MODEL 406229K984062 · DYB | 510(k) clearances |
| Nov 29, 1991 | DAIG FAST CATH(TM) TRANSSEPTAL SHEATH INTRODUCERK911883 · DYB | 510(k) clearances |
| May 7, 1991 | DISPOSABLE PATIENT CABLEK910645 · DSA | 510(k) clearances |
| Sep 17, 1985 | ENDOCARDIAL SCREW-IN LEAD WITH PLATINUM POROUS TIPK852446 · DTB | 510(k) clearances |
| Mar 26, 1982 | CARDIOVASCULAR TEMP. PACEMAKER ELECK820003 · LDF | 510(k) clearances |
| Mar 12, 1982 | PERMANENT & TEMPORARY PACEMAKER ELECTR.K820262 · DTB | 510(k) clearances |
| Feb 4, 1982 | PERMANENT ENDOCARD. UNIPOLAR TINED LEADK812905 · DTB | 510(k) clearances |
| Sep 16, 1981 | PERM. ENDOCARDIAL UNIPOLAR TINED ATRIALK812270 · DTB | 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
