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 Quantitative Medicine, Inc. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Mar 11, 1997: QUANTITATIVE SENTINEL SYSTEM.
| Mar 11, 1997 | QUANTITATIVE SENTINEL SYSTEMK963608 · HGM | 510(k) clearances |
| Aug 1, 1996 | QUANTITATIVE SENTINEL SYSTEMK960109 · HGM | 510(k) clearances |
| Oct 5, 1992 | Q-SDK923255 · GZJ | 510(k) clearances |
| Jun 4, 1992 | Q-MS NEUROMUSCULAR STIMULATORK912462 · IPF | 510(k) clearances |
| Nov 13, 1991 | Q-TENSK912460 · GZJ | 510(k) clearances |
| Nov 13, 1991 | MICRO-QK912463 · GZJ | 510(k) clearances |
| Jan 25, 1991 | QUANTIMETRIX QUAN TEST-RED PROTEIN ASSAY SYSTEMK904603 · CEK | 510(k) clearances |
| Jan 10, 1984 | SENTINEL SYSTEMSK833395 · DXG | 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
