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., part of Becton DickinsonLabelled 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 USCI with 12 510(k) clearances. The most recent is a 510(k) clearance dated Aug 10, 1995: USCI INPUT INTRODUCER SET.
| Aug 10, 1995 | USCI INPUT INTRODUCER SETK940092 · DYB | 510(k) clearances |
| Dec 21, 1988 | USCI DORROS INFUSION/PROBING CATHETERK884209 · DQY | 510(k) clearances |
| Dec 20, 1977 | CATHETER, CARDIOVASCULARK771823 · DYG | 510(k) clearances |
| Nov 2, 1977 | TRC STAINLESS STEEL SAFETY SPRING GUIDESK772021 · DQX | 510(k) clearances |
| Nov 2, 1977 | 888 ARTERIAL/VENOUS CATHETER INTRODUCERK771982 · DYB | 510(k) clearances |
| Oct 5, 1977 | PATCH FABRICK770835 · DXZ | 510(k) clearances |
| Apr 26, 1977 | CATHETER,PERCUTANEOUS INTRODUC. & SHEATHK770561 · DYB | 510(k) clearances |
| Feb 25, 1977 | SAUVAGE FILAMENTOUS PROSTHESESK770236 · DSY | 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
