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 Cathlab Corp. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Aug 2, 1991: CATHLAB SILICONE BILIARY BALLOON CATHETER.
| Aug 2, 1991 | CATHLAB SILICONE BILIARY BALLOON CATHETERK910917 · GCA | 510(k) clearances |
| Jun 24, 1991 | CATHLAB SILICONE OCCLUSION BALLOON CATHETERK910916 · DQT | 510(k) clearances |
| Feb 25, 1991 | CATHLAB SILICONE ARTERIAL EMBOLECTOMY CATHETERK905139 · DXE | 510(k) clearances |
| Mar 16, 1990 | MILLER PERCUTANEOUS ANGIOGRAPHIC/SCOPIC IRRI. CATHK897051 · DQO | 510(k) clearances |
| Mar 14, 1990 | 3F AND 4F IRRIGATION EMBOLECTOMY CATHETERSK897184 · DXE | 510(k) clearances |
| Sep 26, 1989 | SILICONE FLOW-DIRECTED THERMODILUTION CATHETERK893435 · DYG | 510(k) clearances |
| Aug 1, 1989 | SILICONE BI-LUMEN IRRIGATION EMBOLECTOMY CATH.K893680 · DXE | 510(k) clearances |
| Jun 15, 1988 | EMBOLECTOMY CATHETER(MODIFIED)K881455 · DXE | 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
