Medix Medical Electronics (U.S.A.), Inc.
Medix Medical Electronics (U.S.A.), Inc. holds FDA 510(k) medical device clearances, first cleared 1981, most recent 1986.
Top product codes for Medix Medical Electronics (U.S.A.), Inc.
Recent clearances by Medix Medical Electronics (U.S.A.), Inc.
- K861040 — ENTERNAL INFUSER MULTIPUMP 203
- K861001 — PARENTERAL INFUSER MEDIPUMP 204
- K853393 — INSULIN PUMP INSUMAT 229
- K852433 — INFUSAFE 205 CATOLOG NO. 205.000
- K813562 — SYRINGE DRIVER 209
- K812039 — SPIROMETER 210/211
- K812041 — VENTI-MONITOR MODEL 101
- K812045 — INFANT APNEA MONITOR MODEL 100
- K812040 — OXYGEN MONITOR 140/141
- K812046 — TIDAL VOLUME MONITOR 150
- K812044 — RESPIRATION RATE MONITOR 120/121
- K812042 — INFUSION PUMP MODEL 200/201
- K812037 — TEMPERATURE MONITOR 130/131/133
- K812038 — OXYGEN CONTROLLER MODEL 145
Data sourced from openFDA. This site is unofficial and independent of the FDA.