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.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Lifestream International with 23 510(k) clearances. The most recent is a 510(k) clearance dated Aug 8, 1997: VISION CARDIOPLEGIA DELIVERY SYSTEM.
| Aug 8, 1997 | VISION CARDIOPLEGIA DELIVERY SYSTEMK964571 · DTR | 510(k) clearances |
| Sep 11, 1996 | DIOMED 15, 30, 60 SURGICAL DIODE LASERK962354 · GEX | 510(k) clearances |
| May 13, 1993 | CARDIOTOMY RESERVOIR W/20 MICRON FILITERK920178 · DTN | 510(k) clearances |
| Mar 12, 1993 | AUTOTRANSFUSION SUCTION SETK920618 · CAC | 510(k) clearances |
| May 20, 1992 | AUTOLOGOUS BLOOD PROCESSING SYSTEMK913181 · CAC | 510(k) clearances |
| Dec 23, 1991 | SURGI LIGHT NON-CONTACT FIBERSK914396 · GEX | 510(k) clearances |
| Oct 31, 1991 | TMP PRESSURE ISOLATORR, TMP PRESSURE MONITOR SYSTK912045 · DXS | 510(k) clearances |
| Apr 22, 1991 | MODIFICATION TO MODEL 90-1460 LASER ADAPTERK911523 · GEX | 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
