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 Medical Advances, Inc. with 57 510(k) clearances. The most recent is a 510(k) clearance dated Dec 16, 2002: MODEL 472GE-128: QUADRATURE LOWER EXTREMITY COIL.
| Dec 16, 2002 | MODEL 472GE-128: QUADRATURE LOWER EXTREMITY COILK023084 · MOS | 510(k) clearances |
| Jun 13, 2002 | MODEL 415PH-64/42: PHASED ARRAY SHOULDER COILK021433 · MOS | 510(k) clearances |
| Aug 14, 2001 | MODEL 235GE-64; MULTI PURPOSE FLEX ARRAY COILK011608 · MOS | 510(k) clearances |
| Apr 3, 2001 | MODEL 455GE PHASED ARRAY WRIST COILK010074 · MOS | 510(k) clearances |
| Dec 22, 2000 | MODEL 342GE-64 HIGH RESOLUTION BRAIN COILK003685 · MOS | 510(k) clearances |
| Dec 13, 2000 | MODEL 205GE-64: PATHWAY MRI CAROTID ARRAY COILK003144 · MOS | 510(k) clearances |
| Apr 11, 2000 | MULTI PURPOSE FLEX ARRAY COIL : MODEL 235 SERIESK000345 · MOS | 510(k) clearances |
| Aug 2, 1999 | QUADRATURE LOWER EXTREMITY COIL, MODEL 473PH-64K991724 · MOS | 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
