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 15, 2026, FDA's public records list Aries Medical with 19 510(k) clearances. The most recent is a 510(k) clearance dated Oct 28, 1991: SJM/CAD ISOFLOW(TM) CENTRIFUGAL PUMP 2100CP, MODIF.
| Oct 28, 1991 | SJM/CAD ISOFLOW(TM) CENTRIFUGAL PUMP 2100CP, MODIFK912604 · KFM | 510(k) clearances |
| Dec 21, 1990 | ARIES MELDICAL MODEL 2100HC HANK CRANKK903925 · KFM | 510(k) clearances |
| Aug 23, 1990 | ARIES TAPERSEAL(TM) SHEATHK903442 · DYB | 510(k) clearances |
| Apr 10, 1990 | ARIES 30CC & 50CC INTRA-AORTIC BALLOON & CONT. SYSK895433 · DSP | 510(k) clearances |
| Dec 12, 1988 | ARIES 40CC PERCU. (D/L) INTRA-AORTIC BALLOON CATH.K882289 · DSY | 510(k) clearances |
| Jun 19, 1987 | 40CC PERCUTANEOUS PRE-FURL (D/L) BALLOON CATHETERK864537 · DSP | 510(k) clearances |
| Jun 19, 1987 | 40CC PER. PRE-FURL (S/L) INTRA-AORTIC CATHETERK864994 · DSP | 510(k) clearances |
| May 12, 1987 | 40CC PERCUTANEOUS FURL DOU. LUMEN BALLOON CATHETERK864567 · DSP | 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
