Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Baxter InternationalLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Travenol Laboratories with 207 510(k) clearances. The most recent is a 510(k) clearance dated Dec 24, 1996: COPAXONE (COPOLYMER-1 FOR INJECTION) SELF-INJECTION ADMINISTRATION PACKAGE.
| Dec 24, 1996 | COPAXONE (COPOLYMER-1 FOR INJECTION) SELF-INJECTION ADMINISTRATION PACKAGEK964060 · FMF | 510(k) clearances |
| Feb 22, 1988 | BAXTER BEDSIDE SYSTEMK874181 · FRN | 510(k) clearances |
| Nov 5, 1987 | CONTINU-FLO SOLUTION W/CHECK VALVE 2 Y-INJECT SITEK873894 · FPA | 510(k) clearances |
| Oct 22, 1987 | RESUBMITTED MICRON TRANSFUSION FILTERK873873 · CAK | 510(k) clearances |
| Oct 20, 1987 | AUTOMATIC PERITONEAL DIALYSIS CYCLER SET (5C4437)K873984 · KDJ | 510(k) clearances |
| Oct 13, 1987 | HEMODIALYSIS (SPS), MODEL 550, CODE 5M1309K872364 · FII | 510(k) clearances |
| Sep 30, 1987 | UPGRADED AUTO PERITONEAL DIALYSIS CYCLER SYSTEMK872652 · FKX | 510(k) clearances |
| Sep 4, 1987 | FLO-GARD 6200 VOLUMETRIC INFUSION/PUMPING BLOODK870801 · FRN | 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
