Medical device makerLabelled 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 14, 2026, FDA's public records list EMG Technology with 11 510(k) clearances and 1 device recall. The most recent is a device recall dated Aug 3, 2014: Vac-Assist Suction Units (SUA01 Suction Aspirator Unit w/800 cc Canister). The suctio….
| Aug 3, 2014 | Vac-Assist Suction Units (SUA01 Suction Aspirator Unit w/800 cc Canister). The suction unit is intended for professional use to remove flClass II · suction canister lids may have occluded ports. | Device recalls |
| Sep 1, 2011 | EMG SUCTION UNITK112421 · JCX | 510(k) clearances |
| Nov 19, 2008 | EMG TRITON -COMP,MODEL NCA01-XXX SERIESK072634 · BTI | 510(k) clearances |
| Nov 30, 2006 | EMG AC/DC SUCTION UNITK063448 · JCX | 510(k) clearances |
| Oct 24, 2006 | MIDDLE WHEEL DRIVE POWER CHAIR, CWD01K062888 · ITI | 510(k) clearances |
| Jan 31, 2006 | EMG HANDLE NEBULIZER NB02 SERIESK052438 · CAF | 510(k) clearances |
| Oct 21, 2005 | EMG CTA01-XXX SERIES PURO OXYGEN CONCENTRATORK043520 · CAW | 510(k) clearances |
| Jul 6, 2005 | COMPRESSOR NEBULIZER, MODEL EMG NBA02-XXX SERIESK043238 · CAF | 510(k) clearances |
| Dec 16, 2004 | EMG MODEL SUA01 SUCTION UNITK042349 · JCX | 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
