Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United KingdomLabelled 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 Huntleigh Technology with 23 510(k) clearances. The most recent is a 510(k) clearance dated Nov 10, 1999: AKRON ATP9 TRACTION MACHINE.
| Nov 10, 1999 | AKRON ATP9 TRACTION MACHINEK992733 · ITH | 510(k) clearances |
| Feb 21, 1997 | RHEO DOPPLEX II (RD 2)K964699 · IYN | 510(k) clearances |
| Jun 28, 1993 | OP3/VP4K924516 · HGL | 510(k) clearances |
| May 28, 1991 | FLOWPLUS AC330 PUMP GARMENTSK910188 · JOW | 510(k) clearances |
| Aug 22, 1990 | MULTI DOPPLEX, MD-1K900882 · JAF | 510(k) clearances |
| Apr 25, 1990 | HUNTLEIGH FETAL DOPPLER, FD-1 & DOPCORD, D140K900618 · KNG | 510(k) clearances |
| Mar 29, 1989 | HUNTLEIGH DYNAMIC FLOTATION SYSTEMK890012 · FNM | 510(k) clearances |
| Jan 12, 1989 | DOPCORD PPGK884451 · JOM | 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
