Intertech/Ohio is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intertech/Ohio - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Intertech/Ohio has 10 FDA 510(k) cleared anesthesiology devices. Based in Fort Myers, US.
Historical record: 10 cleared submissions from 1986 to 1989.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Intertech/Ohio
10 devices
Cleared
Oct 19, 1989
INTERTECH METERED DOSE ELBOW
Anesthesiology
62d
Cleared
Mar 01, 1989
INTERTECH UNIVERSAL HYDROPHOBIC FILTER
General Hospital
37d
Cleared
Dec 16, 1988
PEDIATRIC HUMIDIFIER TUBE W/ TEMPERATURE PORT
Anesthesiology
50d
Cleared
Nov 16, 1988
ADULT RESUSCITATOR WITH MASK AND FILTER
Anesthesiology
20d
Cleared
Jul 08, 1988
RESUSCITATOR VALVE ASSEMBLY W/FILTER
Anesthesiology
44d
Cleared
Feb 29, 1988
FIRST RESPONSE PEDIATRIC EMERGENCY RESUSCITATOR
Anesthesiology
31d
Cleared
Aug 20, 1986
PATIENT GAS SAMPLING KIT/5STAND ALONE VERSIONS
Anesthesiology
9d
Cleared
Jun 30, 1986
HEAT/MOISTURE EXCHANGER, HME, W/INTEGRAL FILTER
Anesthesiology
33d
Cleared
Mar 28, 1986
90 DEGREE ELBOW & STRAIGHT CONNECTOR
Anesthesiology
35d
Cleared
Mar 27, 1986
STRAIGHT ADAPT W/TEMP SENSING PORT/CLOSURE PLUG
Anesthesiology
8d