Intl. Medical Devices , Ltd.
Intl. Medical Devices , Ltd. holds FDA 510(k) medical device clearances, first cleared 1979, most recent 1992.
Top product codes for Intl. Medical Devices , Ltd.
Recent clearances by Intl. Medical Devices , Ltd.
- K913540 — PEDIA-THOR THORACOSTOMY KIT
- K913541 — NEO-THOR THORACOSTOMY KIT
- K913539 — THORACIC CATHTER STYLET
- K913542 — THORACIC CATHETER WITH GUIDE
- K913543 — THORACIC CATHETER STYLET
- K862909 — RE-TRAKE WEISS EMERGENCY AIRWAY & THORACIC SYSTEM
- K850398 — NU-CATH EMERGENCY KIT
- K843785 — WISSS PEDIATRIC TRACH- TUBE W/OBTURATOR
- K842666 — NU-THOR THORACOSTOMY KIT
- K840925 — PEDIA-TRAKE CRICOTHYROTOMY KIT
- K820778 — RESPIRATION MONITOR 1000
- K790650 — WEISS EMERGENCY AIRWAY SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.