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 BaxterLabelled by claude-sonnet-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 14, 2026, FDA's public records list Protocol Systems with 15 510(k) clearances. The most recent is a 510(k) clearance dated Nov 21, 2000: MICROPAQ, MODELS 402 AND 404.
| Nov 21, 2000 | MICROPAQ, MODELS 402 AND 404K002725 · DRT | 510(k) clearances |
| Nov 7, 1997 | ACUITY CENTRAL STATIONK972121 · MLD | 510(k) clearances |
| Feb 2, 1996 | PROPAQ ENCORE 200 SERIES MONITOR WITH NEONATAL MODE AND IMPEDANCE PNEUMOGRAPHY OPTIONSK951246 · FLS | 510(k) clearances |
| May 10, 1995 | PROPAQ 200 MONITORK945071 · DRT | 510(k) clearances |
| Dec 5, 1994 | MODEL ACUITY CENTRAL STATIONK935846 · DSI | 510(k) clearances |
| Sep 1, 1994 | PROPAQ ECG TELEMETRY OPTIONK934711 · DRG | 510(k) clearances |
| Mar 23, 1993 | PROPAQ MONITORS, MODIFICATIONK921497 · CCK | 510(k) clearances |
| Jan 10, 1992 | PROPAQ 102,104,106,102EL,104EL,&106ELK914838 · MHX | 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
