Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of BaxterLabelled by claude-sonnet-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 Burdick with 44 510(k) clearances. The most recent is a 510(k) clearance dated May 22, 1996: QUEST EXERCISE STRESS SYSTEM.
| May 22, 1996 | QUEST EXERCISE STRESS SYSTEMK952417 · DSI | 510(k) clearances |
| May 3, 1996 | BURDICK 200 PULSE OXIMETERK954267 · DQA | 510(k) clearances |
| Apr 23, 1996 | ECLIPSE 4 ELECTROCARDIOGRAPHK946281 · LOS | 510(k) clearances |
| Jul 3, 1995 | PC HOLTER SCANNING SYSTEM SIMPLICITY, ALTAIR 8200, 8300, 8400K945985 · DQK | 510(k) clearances |
| May 17, 1995 | ECLIPSE 4 ELECTROCARDIOGRAPHK943959 · LOS | 510(k) clearances |
| Dec 5, 1994 | ALTAIR-DISC RECORDERK942565 · DQK | 510(k) clearances |
| Oct 13, 1994 | BURDICK PRO2 OXIMETERK941351 · DQA | 510(k) clearances |
| Aug 5, 1994 | ALTAIR 6100 CASSETTE RECORDERK942438 · DSH | 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
