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 Magna Advanced Technologies, Inc. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Aug 19, 1999: MAGNATEK 30.
| Aug 19, 1999 | MAGNATEK 30K991819 · DQA | 510(k) clearances |
| Oct 2, 1998 | MAGNATEK 40K982907 · DQA | 510(k) clearances |
| Sep 22, 1998 | MAGNATEK80K983114 · CCK | 510(k) clearances |
| Sep 18, 1998 | MTEK-1400K982846 · CCK | 510(k) clearances |
| Sep 17, 1998 | MTEK-1000K982405 · DQA | 510(k) clearances |
| Jul 9, 1998 | MAGNATEK C-300K981310 · GEI | 510(k) clearances |
| Jun 24, 1998 | MAGNATEK ELECTROSURGICAL UNITS MODELS, ESU-10, ESU-15K981416 · GEI | 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
