Itl Corporation Pty, Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K153472 | Quiver Laparoscopic Extendable | June 23, 2016 |
| K021941 | SAMPLOK LUER KIT | July 2, 2002 |
| K021017 | LEESPEC DISPOSABLE VAGINAL SPECULUM | June 19, 2002 |
| K000777 | SAMPLOK | April 11, 2000 |
| K991404 | PLATYPUS AV FISTULA NEEDLE PROTECTOR (AVFNP) | May 14, 1999 |