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 Rozinn Electronics with 6 510(k) clearances. The most recent is a 510(k) clearance dated Sep 15, 2006: TELEPHONE ELECTROCARDIOGRAPH TRANSMITTER AND RECEIVER, TTM FOR WINDOWS +.
| Sep 15, 2006 | TELEPHONE ELECTROCARDIOGRAPH TRANSMITTER AND RECEIVER, TTM FOR WINDOWS +K061780 · DXH | 510(k) clearances |
| Sep 22, 2004 | HOLTER PLUSK042463 · DQK | 510(k) clearances |
| Oct 24, 2002 | CARDIO ID+(RZ153+)K022540 · DSH | 510(k) clearances |
| Jul 24, 2002 | ABP FOR WINDOWSK021517 · DSK | 510(k) clearances |
| Apr 5, 2002 | NETLINK/NETSCANK020213 · DXH | 510(k) clearances |
| Oct 22, 1990 | ROZINN 151K903331 · DSH | 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
