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 Schneider-Shiley (USA) with 9 510(k) clearances. The most recent is a 510(k) clearance dated Jan 24, 1989: SOFTRAC-PTA PERIPHERAL DILATATION CATHETER.
| Jan 24, 1989 | SOFTRAC-PTA PERIPHERAL DILATATION CATHETERK882826 · LIT | 510(k) clearances |
| Jul 28, 1988 | MODIFIED PERIPHERAL DILATATION CATHETERSK875175 · LIT | 510(k) clearances |
| May 16, 1988 | SOFTRAC-PTA(TM) PERIPHERAL DILATATION CATHETERK881197 · LIT | 510(k) clearances |
| Mar 28, 1988 | MODIFIED SCHNEIDER-SHILEY WIRE TORQUERK875323 · DQX | 510(k) clearances |
| Mar 28, 1988 | MODIFIED SCHNEIDER-SHILEY PRESSURE MANOMETERK875322 · KRK | 510(k) clearances |
| Mar 25, 1988 | MODIFIED SCHNEIDER SHILEY INFLATION SYRINGESK875324 · DXT | 510(k) clearances |
| Mar 25, 1988 | MODIFIED SELDINGER INITIAL PUNCTURE INSTRUMENTK875327 · DRE | 510(k) clearances |
| Feb 18, 1988 | MODIFIED OCCLUDER/FLUSHING CATHETER STOPCOCKK875325 · DQO | 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
