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 Tronomed, Inc. with 12 510(k) clearances. The most recent is a 510(k) clearance dated Jan 11, 1996: TRONOMATE PATIENT CABLE & LEADWIRE SYSTEM.
| Jan 11, 1996 | TRONOMATE PATIENT CABLE & LEADWIRE SYSTEMK952659 · DSA | 510(k) clearances |
| Sep 18, 1985 | LIFELINC LEADWIREK853303 · BZQ | 510(k) clearances |
| Sep 10, 1985 | LIFE LINC PATIENT CABLEK853452 · BZQ | 510(k) clearances |
| Jul 24, 1985 | HIGH PRESSURE FLEX. CONNECTING TUBINGK841092 · DXT | 510(k) clearances |
| Jan 16, 1980 | 3&4 WAY PLASTIC STOPCOCKS, NONSTERILEK792125 · FMG | 510(k) clearances |
| Jan 16, 1980 | TANDEM ASSEMBLED 3&4 WAY STOPCOCKSK792124 · FMG | 510(k) clearances |
| Jan 16, 1980 | STERILE EXTENSION TUBES INDIV. PKG.K792128 · FMG | 510(k) clearances |
| Jan 16, 1980 | PLAS. STCK. W/EXTENSION TUBE/STERILEK792127 · FMG | 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
