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 Clincal Instruments Corp. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Feb 25, 1991: EMBOLECTOMY CATHETER.
| Feb 25, 1991 | EMBOLECTOMY CATHETERK902327 · DXE | 510(k) clearances |
| May 28, 1986 | CAROTID BYPASS SHUNTK860742 · DWF | 510(k) clearances |
| May 28, 1986 | CAROTID BYPASS SHUNT WITH SAMPLING ARMK860743 · DWF | 510(k) clearances |
| Nov 26, 1985 | TWEETHEART #102 FETAL/NEONATAL HEARTBEAT ANNUNCIATK852704 · HGM | 510(k) clearances |
| Aug 5, 1985 | OCCLUSION & OCCLUSION-IRRIGATIONK844918 · DQT | 510(k) clearances |
| Jul 9, 1982 | MULTILUMEN INTRAVENOUS INFUSION CATHETERK821220 · GBP | 510(k) clearances |
| Feb 1, 1979 | INTRODUCERSK790034 · DYB | 510(k) clearances |
| Dec 20, 1977 | SWAN GANZK771043 · DYG | 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
