Medix Medical Electronics (U.S.A.), Inc.

FDA Regulatory Profile

Medix Medical Electronics (U.S.A.), Inc. appears in FDA public data with 0 recalls, 14 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 23, 1986.

Summary

Total Recalls
0
510(k) Clearances
14
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K861040ENTERNAL INFUSER MULTIPUMP 203June 23, 1986
K861001PARENTERAL INFUSER MEDIPUMP 204June 12, 1986
K853393INSULIN PUMP INSUMAT 229November 18, 1985
K852433INFUSAFE 205 CATOLOG NO. 205.000June 27, 1985
K813562SYRINGE DRIVER 209February 1, 1982
K812041VENTI-MONITOR MODEL 101September 25, 1981
K812039SPIROMETER 210/211September 25, 1981
K812045INFANT APNEA MONITOR MODEL 100September 24, 1981
K812040OXYGEN MONITOR 140/141September 21, 1981
K812046TIDAL VOLUME MONITOR 150August 7, 1981
K812044RESPIRATION RATE MONITOR 120/121August 4, 1981
K812042INFUSION PUMP MODEL 200/201July 31, 1981
K812037TEMPERATURE MONITOR 130/131/133July 28, 1981
K812038OXYGEN CONTROLLER MODEL 145July 21, 1981