Siemens Medical Electronics - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
Siemens Medical Electronics has 15 FDA 510(k) cleared medical devices. Based in Danvers, US.
Historical record: 15 cleared submissions from 1988 to 1995. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Siemens Medical Electronics Filter by specialty or product code using the sidebar.
15 devices
Cleared
Apr 07, 1995
SIEMENS CLINICAL WORK STATION
Cardiovascular
533d
Cleared
May 07, 1993
SIEMENS SIRECUST 700 BEDSIDES/ACCESSORIES, MODIFI
Cardiovascular
378d
Cleared
Mar 02, 1993
SIEMENS SIRECUST PENTA SYSTEM AND ACCESSORIES
Cardiovascular
392d
Cleared
Nov 06, 1992
SIEMENS NP NONINVASIVE BLOOD PRESS MEASUREMENT SYS
Cardiovascular
381d
Cleared
Apr 23, 1992
SIEMENS RADIOTOM 904 & 904E ELECTROSURGERY UNIT
General & Plastic Surgery
349d
Cleared
Oct 30, 1991
SIEMENS MICRO2 PULSE OXIMETER
Anesthesiology
85d
Cleared
Mar 11, 1991
SIEMENS ETCO2 CARTRIDGE
Anesthesiology
74d
Cleared
Jun 28, 1990
SIEMENS SIRECUST 1481T, DIGITAL TELEMETRY SYSTEM
Cardiovascular
156d
Cleared
May 30, 1990
SIEMENS SIRECUST 732, PATIENT MONITOR
Cardiovascular
41d
Cleared
Oct 02, 1989
SIEMENS SIRECUST 730, PATIENT MONITOR W/ARRHYTHMIA
Cardiovascular
76d
Cleared
Sep 29, 1989
SIEMENS SIRECUST TRANSCUTANEOUS CARBON DIOXIDE
Anesthesiology
196d
Cleared
Aug 03, 1989
SIEMENS SAO2 + PULS OXIMETRY CARTRIDGE
Anesthesiology
91d