Protocol Systems, Inc.
Protocol Systems, Inc. holds FDA 510(k) medical device clearances, first cleared 1988, most recent 2000.
Top product codes for Protocol Systems, Inc.
Recent clearances by Protocol Systems, Inc.
- K002725 — MICROPAQ, MODELS 402 AND 404
- K972121 — ACUITY CENTRAL STATION
- K951246 — PROPAQ ENCORE 200 SERIES MONITOR WITH NEONATAL MODE AND IMPEDANCE PNEUMOGRAPHY OPTIONS
- K945071 — PROPAQ 200 MONITOR
- K935846 — MODEL ACUITY CENTRAL STATION
- K934711 — PROPAQ ECG TELEMETRY OPTION
- K921497 — PROPAQ MONITORS, MODIFICATION
- K914838 — PROPAQ 102,104,106,102EL,104EL,&106EL
- K913193 — MODEL 100 CENTRAL STATION
- K910882 — PROPAQ 102EL, 104EL AND 106EL
- K910772 — PROPAQ 102, 104 AND 106
- K902730 — SPO2 OPTION
- K894607 — PAQ10 PAPER CHART RECORDER
- K884320 — PROPAQ 106(TM)
- K882085 — PROPAQ 104(TM)
Data sourced from openFDA. This site is unofficial and independent of the FDA.