Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of PhilipsLabelled 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 13, 2026, FDA's public records list Quinton with 164 510(k) clearances. The most recent is a 510(k) clearance dated Sep 5, 2003: PYRAMIS ECG MANAGEMENT SYSTEM MODEL NUMBERS, 92600 AND 92601.
| Date | Record | Source |
|---|---|---|
| Sep 5, 2003 | PYRAMIS ECG MANAGEMENT SYSTEM MODEL NUMBERS, 92600 AND 92601K032038 · DQK | 510(k) clearances |
| Sep 4, 2002 | QUINTON Q-CATH, MODEL 000460K021906 · DQK | 510(k) clearances |
| Jan 25, 2001 | Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 000503K003576 · DSI | 510(k) clearances |
| Aug 9, 2000 | QUINTON Q-STRESS, MODEL 000483K001492 · DPS | 510(k) clearances |
| Mar 6, 2000 | Q-TEL TELEMETRY SYSTEM V. 6.0 (ST)K992908 · DSI | 510(k) clearances |
| Apr 29, 1999 | QUINTON MEDTRACK CR PLUS TREADMILLK990866 · ISD | 510(k) clearances |
| Aug 25, 1997 | VIEWCATH 3-D CATHETER PULLBACKK971397 · ITX | 510(k) clearances |
| Aug 13, 1997 | SYNERGY CARDIOLOGY INFORMATION SYSTEM (00431)K964784 · DPS | 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
