Roche Medical Electronics, Inc.
Roche Medical Electronics, Inc. holds FDA 510(k) medical device clearances, first cleared 1976, most recent 1979.
Top product codes for Roche Medical Electronics, Inc.
Recent clearances by Roche Medical Electronics, Inc.
- K791559 — ROCHE SENSOR ADAPTOR
- K791035 — FETASONDE FETAL ACTIVITY MONITOR
- K791036 — FETASONDE UTERINE WORK MONITOR
- K791037 — FETASONDE LABOR STATUS DISPLAY
- K791038 — FETASONDE UTERINE ACTIVITY MONITOR
- K791039 — FETASONDE FETAL HEART RATE VARIABILITY
- K790761 — FETASONDE MODEL 2108
- K790421 — ROCHE LACTATE ANALYZER 640
- K782088 — MONITOR, HEART RATE MODEL 105
- K782089 — MONITOR, HEART RATE MODEL 103
- K781271 — MONITOR, PO2, INTRAVASCULAR
- K780179 — LIQUID SCINTILLATION COUNTER
- K771816 — ROCHE AXISCAN 5
- K771478 — INFUSION PUMP #6202
- K761057 — ARTERIOSONDE BLOOD PRESS. MNTR. (#1020)
- K760919 — MODEL 2106 FETA SONDE FETAL MONITOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.