Intl. Medical Devices , Ltd.

12 FDA 510(k) medical device clearances.

Top product codes for Intl. Medical Devices , Ltd.

BTO — Anesthesiology 3 devices
FMF — General Hospital 2 devices
GBX — General, Plastic Surgery 2 devices
BWC — Anesthesiology 1 device
BZQ — Anesthesiology 1 device
DRB — Cardiovascular 1 device
FOZ — General Hospital 1 device
KGZ — General, Plastic Surgery 1 device

Recent clearances by Intl. Medical Devices , Ltd.

K913540 — PEDIA-THOR THORACOSTOMY KIT FMF · 1992-04-09
K913541 — NEO-THOR THORACOSTOMY KIT FMF · 1992-04-09
K913539 — THORACIC CATHTER STYLET GBX · 1992-01-21
K913542 — THORACIC CATHETER WITH GUIDE GBX · 1992-01-21
K913543 — THORACIC CATHETER STYLET DRB · 1991-10-04
K862909 — RE-TRAKE WEISS EMERGENCY AIRWAY & THORACIC SYSTEM BTO · 1986-09-09
K850398 — NU-CATH EMERGENCY KIT FOZ · 1985-03-27
K843785 — WISSS PEDIATRIC TRACH- TUBE W/OBTURATOR BTO · 1984-10-23
K842666 — NU-THOR THORACOSTOMY KIT KGZ · 1984-09-20
K840925 — PEDIA-TRAKE CRICOTHYROTOMY KIT BTO · 1984-05-02
K820778 — RESPIRATION MONITOR 1000 BZQ · 1982-05-03
K790650 — WEISS EMERGENCY AIRWAY SYSTEM BWC · 1979-06-27

Data sourced from openFDA. This site is unofficial and independent of the FDA.