Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Interrad Medical, Inc. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Apr 12, 2021: SecurAcath.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Apr 12, 2021 | SecurAcathK210629 · OKC | 510(k) clearances |
| Jul 9, 2019 | SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8FK180994 · KMK | 510(k) clearances |
| Jun 26, 2018 | SecurAcathK180769 · OKC | 510(k) clearances |
| Apr 27, 2012 | SECURACATHK120935 · OKC | 510(k) clearances |
| Jul 9, 2010 | SECURACATH UNIVERSALK092306 · LJS | 510(k) clearances |
| Mar 4, 2009 | MODIFICATION TO SECURACATH, MODEL: SPK01K083081 · OKC | 510(k) clearances |
| Sep 30, 2008 | SECURACATH CATHETER, MODEL SPK01K082047 · OKC | 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
