Epic Medical Equipment Services, Inc. - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Epic Medical Equipment Services, Inc. has 13 FDA 510(k) cleared anesthesiology devices. Based in Plano, US.
Historical record: 13 cleared submissions from 1996 to 2001.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
13 devices
Cleared
Oct 17, 2001
FLEXI-SITE SP02 EAR SENSOR
Anesthesiology
85d
Cleared
May 24, 2001
SPO2 WRAP SENSOR
Anesthesiology
253d
Cleared
Mar 23, 2001
FLEXI-SITE SP02 EAR SENSOR
Anesthesiology
11d
Cleared
Aug 22, 2000
EPIC SPO2 FINGER SENSOR, MODEL E412-20
Anesthesiology
29d
Cleared
Jun 05, 2000
STAT-SHELL DISPOSABLE SP02 SENSOR
Anesthesiology
83d
Cleared
Jan 18, 2000
TRANSDUCERS FOR ULTRASOUND AND TOCODYNAMOMETER FETAL MONITORING
Radiology
151d
Cleared
Dec 22, 1999
STAT-SHELL DISPOSABLE SPO2 SENSOR
Anesthesiology
184d
Cleared
Dec 22, 1999
SPO2 WRAP SENSOR
Anesthesiology
174d
Cleared
Apr 09, 1999
EPIC SPO2 FINGER SENSOR, MODEL E403-09, E412-09 AND EPIC OXIMETER CABLE,...
Anesthesiology
88d
Cleared
Apr 30, 1998
E100 SERIES SPO2 SENSORS
Anesthesiology
472d
Cleared
Jul 16, 1997
OXIMETER PRE-AMP CABLE
Anesthesiology
204d
Cleared
Feb 21, 1997
FLEXI-SITE (E203-01)/ FLEXI-FIT (E300)
Anesthesiology
135d
Cleared
Sep 12, 1996
E100A PULSE OXIMETER FINGER SENSOR/PROBE
Anesthesiology
373d