Product code MWI— Cardiovascular
M2376A DEVICELINK SYSTEM
- Classification name
- Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
- Device class
- Class 2
- Regulation
- 21 CFR 870.2300
- Advisory panel
- Cardiovascular
- Total cleared
- 308
- First cleared
- Most recent
Clearances under product code MWI — page 4
301–308 of 308- K002009 — HP M2376A DEVICE LINK SYSTEM, MODEL M2376A
- K001265 — WELCH ALLYN INSTRUMENT INTERFACE MODULE
- K001776 — MODIFICATION TO HP M2376A DEVICE LINK SYSTEM, MODEL M2376A
- K001020 — 8100 VITAL SIGNS MONITOR
- K000635 — MODIFICATION TO HP M2376A DEVICE LINK SYSTEM
- K992638 — DINAMAP PRO SERIES MONITOR, MODELS 100, 200, 300, 400
- K983928 — KODAK HOME HEALTH MONITORING SYSTEM
- K980688 — INTEGRITI PATIENT MONITOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.