Medical Device Manufacturer · US , Fort Myers , FL

Intertech/Ohio - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1986

10

Total

10

Cleared

0

Denied

FDA 510(k) Regulatory Record - Intertech/Ohio Anesthesiology ✕

9 devices

1-9 of 9

Cleared Oct 19, 1989

INTERTECH METERED DOSE ELBOW

Anesthesiology · 62d

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