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 Grandcor Medical Systems with 8 510(k) clearances. The most recent is a 510(k) clearance dated May 6, 1991: SPIROSCOPE.
| May 6, 1991 | SPIROSCOPEK905480 · BZC | 510(k) clearances |
| Mar 13, 1990 | GRANDCOR/CARDIOLINE ECT STRESS TESTINGK895547 · DSI | 510(k) clearances |
| Oct 17, 1988 | CARDIOMEGA-TK883410 · DSI | 510(k) clearances |
| Jun 12, 1987 | CARDIO-MEGA SYSTEMK871890 · DSI | 510(k) clearances |
| May 11, 1987 | APPLICARD SYSTEM (ECG ELECTRODE SYSTEM)K864260 · DRX | 510(k) clearances |
| Feb 19, 1987 | APPLISCOPEK864978 · DPS | 510(k) clearances |
| Jan 21, 1987 | APPLIDYNK864581 · ISD | 510(k) clearances |
| Jul 1, 1986 | CARDIO PORT 500 24-H ECG AMBULATORY MONITOR SYSTEMK862375 · DSI | 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
