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 Harbor Medical Devices with 7 510(k) clearances. The most recent is a 510(k) clearance dated May 15, 1989: HARBORIN CENTRAL VENOUS CATHETER.
| May 15, 1989 | HARBORIN CENTRAL VENOUS CATHETERK884628 · DQR | 510(k) clearances |
| Apr 21, 1989 | SINGLE LUMEN S.E.A.-PORT VASCULAR ACCESS SYSTEMK890518 · LJT | 510(k) clearances |
| Dec 13, 1988 | HARBOR S.E.A.-PORT SURGICAL ACCESSORY KITK882657 · DYB | 510(k) clearances |
| Jul 28, 1988 | HARBOR CENTRAL VENOUS CATHETERK881884 · DQR | 510(k) clearances |
| Jun 9, 1988 | S.E.A.-PORT(TM) VASCULAR ACCESS SYSTEMK882190 · LJT | 510(k) clearances |
| Feb 19, 1988 | SEA - PORT INFUSION SETK880297 · LJT | 510(k) clearances |
| Jan 14, 1988 | HYPODERMIC NEEDLES, SINGLE LUMENK874414 · FMI | 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
