Intertech/Ohio
Intertech/Ohio holds FDA 510(k) medical device clearances, first cleared 1986, most recent 1989.
Top product codes for Intertech/Ohio
Recent clearances by Intertech/Ohio
- K895144 — INTERTECH METERED DOSE ELBOW
- K890346 — INTERTECH UNIVERSAL HYDROPHOBIC FILTER
- K884525 — PEDIATRIC HUMIDIFIER TUBE W/ TEMPERATURE PORT
- K884526 — ADULT RESUSCITATOR WITH MASK AND FILTER
- K882204 — RESUSCITATOR VALVE ASSEMBLY W/FILTER
- K880394 — FIRST RESPONSE PEDIATRIC EMERGENCY RESUSCITATOR
- K863033 — PATIENT GAS SAMPLING KIT/5STAND ALONE VERSIONS
- K862020 — HEAT/MOISTURE EXCHANGER, HME, W/INTEGRAL FILTER
- K860650 — 90 DEGREE ELBOW & STRAIGHT CONNECTOR
- K861056 — STRAIGHT ADAPT W/TEMP SENSING PORT/CLOSURE PLUG
Data sourced from openFDA. This site is unofficial and independent of the FDA.