Intl. Medical Devices , Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 12
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K913540 | PEDIA-THOR THORACOSTOMY KIT | April 9, 1992 |
| K913541 | NEO-THOR THORACOSTOMY KIT | April 9, 1992 |
| K913542 | THORACIC CATHETER WITH GUIDE | January 21, 1992 |
| K913539 | THORACIC CATHTER STYLET | January 21, 1992 |
| K913543 | THORACIC CATHETER STYLET | October 4, 1991 |
| K862909 | RE-TRAKE WEISS EMERGENCY AIRWAY & THORACIC SYSTEM | September 9, 1986 |
| K850398 | NU-CATH EMERGENCY KIT | March 27, 1985 |
| K843785 | WISSS PEDIATRIC TRACH- TUBE W/OBTURATOR | October 23, 1984 |
| K842666 | NU-THOR THORACOSTOMY KIT | September 20, 1984 |
| K840925 | PEDIA-TRAKE CRICOTHYROTOMY KIT | May 2, 1984 |
| K820778 | RESPIRATION MONITOR 1000 | May 3, 1982 |
| K790650 | WEISS EMERGENCY AIRWAY SYSTEM | June 27, 1979 |