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 13, 2026, FDA's public records list HemoCleanse, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Dec 30, 1999: THERMOCHEM-HT SYSTEM.
| Date | Record | Source |
|---|---|---|
| Dec 30, 1999 | THERMOCHEM-HT SYSTEMK993330 · MLW | 510(k) clearances |
| Sep 10, 1999 | BIOLOGIC-DT SYSTEM (BIOLOGIC-DT-1000 WITH DT-1000-TK)K992196 · FLD | 510(k) clearances |
| Aug 13, 1999 | BIOLOGIC-DT MACHINE, MODEL DT-1000 AND BIOLOGIC-DT TREATMENT KIT, MODEL DT-1000-TKK984546 · FLD | 510(k) clearances |
| Feb 15, 1996 | BIOLOGIC-DT SYSTEMK953751 · FLD | 510(k) clearances |
| Sep 30, 1994 | BIOLOGIC DT-1000 MACHINEK923046 · KNT | 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
