Pro-Tech Services, Inc. - FDA 510(k) Cleared Devices
7
Total
6
Cleared
0
Denied
Pro-Tech Services, Inc. has 6 FDA 510(k) cleared medical devices. Based in Woodinville, US.
Historical record: 6 cleared submissions from 1994 to 2005. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Pro-Tech Services, Inc. Filter by specialty or product code using the sidebar.
7 devices
Cleared
Dec 13, 2005
PRO-FLOW MULTIPURPOSE CANNULA
Anesthesiology
42d
Cleared
Jun 30, 2004
PORTABLE SLEEP DATA RECORDER (PSDR)
Anesthesiology
250d
Cleared
Apr 22, 2002
MODIFICATION EZ-1 SYSTEM REPIRATORY SENSORS
Anesthesiology
147d
Cleared
Jul 13, 1998
PRESSURE TRANSDUCER AIRFLOW SENSOR
Anesthesiology
12d
Cleared
Oct 02, 1997
SENSOR AMPLIFIER
Neurology
91d
Cleared
Sep 17, 1996
THERMISTOR CANNULA STYLE,SINGLE ELEMENT,ADAM SHELL THERMISTOR AIRFLOW SENSOR
Anesthesiology
200d
Cleared
Oct 14, 1994
ADAM SHELL THERMOCOUPLE ASSEMBLY
Anesthesiology
49d