Roche Medical Electronics, Inc. - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Roche Medical Electronics, Inc. has 16 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 16 cleared submissions from 1976 to 1979. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Roche Medical Electronics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Roche Medical Electronics, Inc.
16 devices
Cleared
Nov 21, 1979
ROCHE SENSOR ADAPTOR
Anesthesiology
96d
Cleared
Sep 04, 1979
FETASONDE FETAL ACTIVITY MONITOR
Obstetrics & Gynecology
91d
Cleared
Sep 04, 1979
FETASONDE UTERINE WORK MONITOR
Obstetrics & Gynecology
91d
Cleared
Sep 04, 1979
FETASONDE LABOR STATUS DISPLAY
Obstetrics & Gynecology
91d
Cleared
Sep 04, 1979
FETASONDE UTERINE ACTIVITY MONITOR
Obstetrics & Gynecology
91d
Cleared
Sep 04, 1979
FETASONDE FETAL HEART RATE VARIABILITY
Obstetrics & Gynecology
91d
Cleared
Jun 01, 1979
FETASONDE MODEL 2108
Obstetrics & Gynecology
45d
Cleared
May 15, 1979
ROCHE LACTATE ANALYZER 640
Chemistry
76d
Cleared
Jan 04, 1979
MONITOR, HEART RATE MODEL 105
Cardiovascular
21d
Cleared
Jan 04, 1979
MONITOR, HEART RATE MODEL 103
Cardiovascular
21d
Cleared
Oct 12, 1978
MONITOR, PO2, INTRAVASCULAR
Anesthesiology
80d
Cleared
Feb 23, 1978
LIQUID SCINTILLATION COUNTER
Toxicology
20d