National Catheter Co. Div. Mallinckrodt
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K802918 | ANTHRON CATHETER SET | April 21, 1981 |
| K802505 | DOUBLE LUMEN TRACHEAL TUBE | March 13, 1981 |
| K810321 | REINFORCED TRACHEOSTOMY TUBE SET(TENTAT) | March 4, 1981 |
| K801924 | HI-LO TEMP GEN. PURPOSE TEMP. PROBE | September 9, 1980 |
| K801005 | MLT TUBE MICROLARYNGEAL TRACHEAL TUBE) | May 23, 1980 |
| K791190 | STETHOSCOPE WITH TEMPERATURE SENSOR | July 6, 1979 |
| K781665 | TUBE, LEATHERMAN/IMBRUCE | December 15, 1978 |
| K770727 | MANIPULATOR & INJECTOR, UTERINE | April 26, 1977 |