Medix Medical Electronics (U.S.A.), Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Medix Medical Electronics (U.S.A.), Inc. has 14 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 14 cleared submissions from 1981 to 1986. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Medix Medical Electronics (U.S.A.), Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medix Medical Electronics (U.S.A.), Inc.
14 devices
Cleared
Jun 23, 1986
ENTERNAL INFUSER MULTIPUMP 203
General Hospital
97d
Cleared
Jun 12, 1986
PARENTERAL INFUSER MEDIPUMP 204
General Hospital
86d
Cleared
Nov 18, 1985
INSULIN PUMP INSUMAT 229
General Hospital
98d
Cleared
Jun 27, 1985
INFUSAFE 205 CATOLOG NO. 205.000
General Hospital
17d
Cleared
Feb 01, 1982
SYRINGE DRIVER 209
General Hospital
41d
Cleared
Sep 25, 1981
SPIROMETER 210/211
Anesthesiology
66d
Cleared
Sep 25, 1981
VENTI-MONITOR MODEL 101
Anesthesiology
66d
Cleared
Sep 24, 1981
INFANT APNEA MONITOR MODEL 100
Anesthesiology
65d
Cleared
Sep 21, 1981
OXYGEN MONITOR 140/141
Anesthesiology
62d
Cleared
Aug 07, 1981
TIDAL VOLUME MONITOR 150
Anesthesiology
17d
Cleared
Aug 04, 1981
RESPIRATION RATE MONITOR 120/121
Anesthesiology
14d
Cleared
Jul 31, 1981
INFUSION PUMP MODEL 200/201
General Hospital
10d