Edentec Corp. - FDA 510(k) Cleared Devices
18
Total
17
Cleared
0
Denied
Edentec Corp. has 17 FDA 510(k) cleared medical devices. Based in Eden Prairie, US.
Historical record: 17 cleared submissions from 1985 to 1996. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Edentec Corp. Filter by specialty or product code using the sidebar.
18 devices
Cleared
Feb 06, 1996
OXIFLOW DIGITAL RECORDER
Anesthesiology
204d
Cleared
Aug 25, 1995
EEE
Anesthesiology
28d
Cleared
Oct 22, 1993
EDENTEC MODEL 3710 I DIGITAL PRINTER
Anesthesiology
555d
Cleared
Jul 02, 1992
EDENTRACE AIRFLOW 3171/SLEEP LAB AIRFLOW 3170
Anesthesiology
316d
Cleared
Aug 29, 1991
EDENTEC MODEL 3711 DIGITAL RECORDER
Cardiovascular
181d
Cleared
Aug 29, 1991
EDENTEC DIGITAL CHARTER MODEL 3710
Cardiovascular
181d
Cleared
Jun 20, 1991
MODIFIED MODELS 2000W AND 2000W OPTION H APNEA MON
Anesthesiology
190d
Cleared
May 15, 1990
EDENTEC MODEL 2000W SYSTEM 700 MONITOR
Anesthesiology
70d
Cleared
Aug 25, 1989
EDENTRACE 670 SYSTEM MULTICHANNEL RECORDER W/OXIM.
Cardiovascular
108d
Cleared
Jun 20, 1989
EDENTEC MODEL 2001 MODULAR MEMORY UNIT (MMU)
Cardiovascular
77d
Cleared
Jun 01, 1989
EDENTEC MODEL 2860 PRESSURE METER
Anesthesiology
76d
Cleared
Feb 01, 1989
EDENTEC MODEL 2000W OPTION S CARDIO-RESP. PROCESS.
Anesthesiology
89d